Linked Data
dbSNP Id:
rs1877447735
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.40644352G>A , CM000675.2:g.40644352G>A | GRCh38 |
| NC_000013.10:g.41218489G>A , CM000675.1:g.41218489G>A | GRCh37 |
| NC_000013.9:g.40116489G>A | NCBI36 |
| NG_023244.1:g.27246C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379561.6:c.630+21231C>T MANE Select | ENSP00000368880.4:n.630+21231C>T | |
| ENST00000655267.1:n.333+21231C>T | ||
| ENST00000660760.1:n.296-11104C>T | ||
| ENST00000379561.5:c.630+21231C>T | ENSP00000368880.4:n.630+21231C>T | |
| NM_002015.3:c.630+21231C>T | NP_002006.2:n.630+21231C>T | |
| XR_941536.1:n.1226+987C>T | ||
| NM_002015.4:c.630+21231C>T MANE Select | NP_002006.2:n.630+21231C>T |