Linked Data
MyVariant Identifiers:
chr5:g.156995964C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.157568956C>A , CM000667.2:g.157568956C>A | GRCh38 |
| NC_000005.9:g.156995964C>A , CM000667.1:g.156995964C>A | GRCh37 |
| NC_000005.8:g.156928542C>A | NCBI36 |
| NG_046960.1:g.11868G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000257527.9:c.180+1939G>T MANE Select | ENSP00000257527.5:n.180+1939G>T | |
| ENST00000257527.8:c.180+1939G>T | ENSP00000257527.4:n.180+1939G>T | |
| ENST00000517905.1:c.180+1939G>T | ENSP00000428654.1:n.180+1939G>T | |
| ENST00000517951.5:c.180+1939G>T | ENSP00000428376.1:n.180+1939G>T | |
| NM_033274.4:c.180+1939G>T | NP_150377.1:n.180+1939G>T | |
| XM_005266003.2:c.180+1939G>T | XP_005266060.1:n.180+1939G>T | |
| NM_033274.5:c.180+1939G>T MANE Select | NP_150377.1:n.180+1939G>T |