Linked Data
ClinVar Variation Id:
313487
ClinVar RCV Id:
RCV000543727
dbSNP Id:
rs761844853
ExAC:
14:64444647 C / T
gnomAD v2:
14-64444647-C-T
gnomAD v3:
14-63977929-C-T
gnomAD v4:
14-63977929-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.63977929C>T , CM000676.2:g.63977929C>T | GRCh38 |
| NC_000014.8:g.64444647C>T , CM000676.1:g.64444647C>T | GRCh37 |
| NC_000014.7:g.63514400C>T | NCBI36 |
| NG_011756.1:g.129965C>T | |
| NG_011756.2:g.221031C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000555002.6:c.1318C>T MANE Select | ENSP00000450831.2:p.His440Tyr | |
| ENST00000674003.1:c.1318C>T | ENSP00000501132.1:p.His440Tyr | |
| ENST00000674144.1:c.1318C>T | ENSP00000501227.1:p.His440Tyr | |
| ENST00000344113.8:c.1318C>T | ENSP00000341781.4:p.His440Tyr | |
| ENST00000357395.7:c.1318C>T | ENSP00000349969.4:p.His440Tyr | |
| ENST00000358025.7:c.1318C>T | ENSP00000350719.3:p.His440Tyr | |
| ENST00000554584.5:c.1318C>T | ENSP00000452570.1:p.His440Tyr | |
| NM_015180.4:c.1318C>T | NP_055995.4:p.His440Tyr | |
| NM_182914.2:c.1318C>T | NP_878918.2:p.His440Tyr | |
| XM_005267454.1:c.1318C>T | XP_005267511.1:p.His440Tyr | |
| XM_005267456.1:c.1318C>T | XP_005267513.1:p.His440Tyr | |
| XM_005267457.1:c.1318C>T | XP_005267514.1:p.His440Tyr | |
| XM_005267458.1:c.1318C>T | XP_005267515.1:p.His440Tyr | |
| XM_005267459.1:c.1318C>T | XP_005267516.1:p.His440Tyr | |
| XM_006720084.2:c.1318C>T | XP_006720147.1:p.His440Tyr | |
| XM_011536574.1:c.1318C>T | XP_011534876.1:p.His440Tyr | |
| XM_011536575.1:c.1318C>T | XP_011534877.1:p.His440Tyr | |
| XM_011536576.1:c.1318C>T | XP_011534878.1:p.His440Tyr | |
| XM_011536577.1:c.1318C>T | XP_011534879.1:p.His440Tyr | |
| XM_011536578.1:c.1318C>T | XP_011534880.1:p.His440Tyr | |
| XM_011536579.1:c.1318C>T | XP_011534881.1:p.His440Tyr | |
| XM_011536580.1:c.1318C>T | XP_011534882.1:p.His440Tyr | |
| XM_011536581.1:c.1318C>T | XP_011534883.1:p.His440Tyr | |
| XM_011536582.1:c.1318C>T | XP_011534884.1:p.His440Tyr | |
| XM_011536584.1:c.1318C>T | XP_011534886.1:p.His440Tyr | |
| XM_011536575.2:c.1318C>T | XP_011534877.1:p.His440Tyr | |
| XM_011536576.2:c.1318C>T | XP_011534878.1:p.His440Tyr | |
| XM_011536577.2:c.1318C>T | XP_011534879.1:p.His440Tyr | |
| XM_011536580.2:c.1318C>T | XP_011534882.1:p.His440Tyr | |
| XM_011536584.2:c.1318C>T | XP_011534886.1:p.His440Tyr | |
| XM_017021101.1:c.1318C>T | XP_016876590.1:p.His440Tyr | |
| XM_017021102.1:c.1249C>T | XP_016876591.1:p.His417Tyr | |
| XR_001750198.1:n.1548C>T | ||
| NM_015180.5:c.1318C>T | NP_055995.4:p.His440Tyr | |
| NM_015180.6:c.1318C>T | NP_055995.4:p.His440Tyr | |
| NM_182914.3:c.1318C>T MANE Select | NP_878918.2:p.His440Tyr |