Linked Data
gnomAD v4:
1-172665834-C-T
COSMIC:
COSM3478426
MyVariant Identifiers:
chr1:g.172634974C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.172665834C>T , CM000663.2:g.172665834C>T | GRCh38 |
| NC_000001.10:g.172634974C>T , CM000663.1:g.172634974C>T | GRCh37 |
| NC_000001.9:g.170901597C>T | NCBI36 |
| NG_007269.1:g.11790C>T , LRG_58:g.11790C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367721.3:c.664C>T MANE Select | ENSP00000356694.2:p.Leu222= | |
| ENST00000340030.4:c.*234C>T | ENSP00000344739.3:n.*234C>T | |
| ENST00000367721.2:c.664C>T | ENSP00000356694.2:p.Leu222= | |
| NM_000639.2:c.664C>T | NP_000630.1:p.Leu222= | |
| NM_001302746.1:c.*234C>T | NP_001289675.1:n.*234C>T | |
| NM_000639.3:c.664C>T MANE Select | NP_000630.1:p.Leu222= | |
| NM_001302746.2:c.*234C>T | NP_001289675.1:n.*234C>T |