dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.160539327T>A , CM000668.2:g.160539327T>A | GRCh38 |
| NC_000006.11:g.160960359T>A , CM000668.1:g.160960359T>A | GRCh37 |
| NC_000006.10:g.160880349T>A | NCBI36 |
| NG_016147.1:g.132049A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000316300.10:c.5735+716A>T MANE Select | ENSP00000321334.6:n.5735+716A>T | |
| ENST00000316300.9:c.5735+716A>T | ENSP00000321334.5:n.5735+716A>T | |
| NM_005577.2:c.5735+716A>T | NP_005568.2:n.5735+716A>T | |
| NM_005577.3:c.5735+716A>T | NP_005568.2:n.5735+716A>T | |
| NM_005577.4:c.5735+716A>T MANE Select | NP_005568.2:n.5735+716A>T |