Linked Data
dbSNP Id:
rs201801648
ExAC:
11:113281457 G / A
gnomAD v2:
11-113281457-G-A
gnomAD v3:
11-113410735-G-A
gnomAD v4:
11-113410735-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.113410735G>A , CM000673.2:g.113410735G>A | GRCh38 |
| NC_000011.9:g.113281457G>A , CM000673.1:g.113281457G>A | GRCh37 |
| NC_000011.8:g.112786667G>A | NCBI36 |
| NG_008841.1:g.69545C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000362072.8:c.1324C>T MANE Select | ENSP00000354859.3:p.His442Tyr | |
| ENST00000346454.7:c.1237C>T | ENSP00000278597.5:p.His413Tyr | |
| ENST00000362072.7:c.1324C>T | ENSP00000354859.3:p.His442Tyr | |
| ENST00000538967.5:c.1330C>T | ENSP00000438215.1:p.His444Tyr | |
| ENST00000542968.5:c.1324C>T | ENSP00000442172.1:p.His442Tyr | |
| ENST00000544518.5:c.1321C>T | ENSP00000441068.1:p.His441Tyr | |
| NM_000795.3:c.1324C>T | NP_000786.1:p.His442Tyr | |
| NM_016574.3:c.1237C>T | NP_057658.2:p.His413Tyr | |
| XM_017017296.2:c.1324C>T | XP_016872785.1:p.His442Tyr | |
| NM_000795.4:c.1324C>T MANE Select | NP_000786.1:p.His442Tyr | |
| NM_016574.4:c.1237C>T | NP_057658.2:p.His413Tyr |