Linked Data
ClinVar Variation Id:
1157470
ClinVar RCV Id:
RCV002241026
dbSNP Id:
rs2135269268
COSMIC:
COSM358602
MyVariant Identifiers:
chr11:g.111959622T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.112088898T>C , CM000673.2:g.112088898T>C | GRCh38 |
| NC_000011.9:g.111959622T>C , CM000673.1:g.111959622T>C | GRCh37 |
| NC_000011.8:g.111464832T>C | NCBI36 |
| NG_012337.2:g.7052T>C | |
| NG_033145.1:g.2901A>G | |
| NG_012337.3:g.7052T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000530923.6:c.201T>C | ENSP00000432946.2:p.Thr67= | |
| ENST00000534010.2:c.201T>C | ENSP00000433202.2:p.Thr67= | |
| ENST00000375549.8:c.201T>C MANE Select | ENSP00000364699.3:p.Thr67= | |
| ENST00000528021.6:c.201T>C | ENSP00000432465.1:p.Thr67= | |
| ENST00000640554.1:c.*273T>C | ENSP00000491141.1:n.*273T>C | |
| ENST00000375549.7:c.201T>C | ENSP00000364699.3:p.Thr67= | |
| ENST00000525291.5:c.84T>C | ENSP00000436669.1:p.Thr28= | |
| ENST00000525987.5:n.206T>C | ||
| ENST00000526592.5:c.201T>C | ENSP00000432005.1:p.Thr67= | |
| ENST00000528021.5:c.201T>C | ENSP00000432465.1:p.Thr67= | |
| ENST00000528048.5:c.169+925T>C | ENSP00000436217.1:n.169+925T>C | |
| ENST00000528182.5:c.201T>C | ENSP00000435475.1:p.Thr67= | |
| ENST00000530923.5:c.191T>C | ||
| ENST00000531744.5:c.201T>C | ENSP00000456957.1:p.Thr67= | |
| ENST00000532699.1:c.201T>C | ENSP00000456434.1:p.Thr67= | |
| ENST00000534010.1:c.32T>C | ||
| ENST00000614349.4:c.201T>C | ENSP00000480666.1:p.Thr67= | |
| NM_001276503.1:c.169+925T>C | NP_001263432.1:n.169+925T>C | |
| NM_001276504.1:c.84T>C | NP_001263433.1:p.Thr28= | |
| NM_001276506.1:c.201T>C | NP_001263435.1:p.Thr67= | |
| NM_003002.3:c.201T>C | NP_002993.1:p.Thr67= | |
| NR_077060.1:n.285T>C | ||
| NM_003002.4:c.201T>C MANE Select | NP_002993.1:p.Thr67= | |
| NM_001276503.2:c.169+925T>C | NP_001263432.1:n.169+925T>C | |
| NM_001276504.2:c.84T>C | NP_001263433.1:p.Thr28= | |
| NM_001276506.2:c.201T>C | NP_001263435.1:p.Thr67= | |
| NR_077060.2:n.236T>C |