Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.149569908G>A , CM000664.2:g.149569908G>A | GRCh38 |
| NC_000002.11:g.150426422G>A , CM000664.1:g.150426422G>A | GRCh37 |
| NC_000002.10:g.150134668G>A | NCBI36 |
| NG_009189.1:g.22909C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303319.10:c.*66C>T MANE Select | ENSP00000301920.5:n.*66C>T | |
| ENST00000303319.9:c.*66C>T | ENSP00000301920.5:n.*66C>T | |
| ENST00000422782.2:c.*66C>T | ENSP00000408331.2:n.*66C>T | |
| ENST00000428879.5:c.*66C>T | ENSP00000389060.1:n.*66C>T | |
| NM_015702.2:c.*66C>T | NP_056517.1:n.*66C>T | |
| NM_015702.3:c.*66C>T MANE Select | NP_056517.1:n.*66C>T |