dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.117897021A>T , CM000670.2:g.117897021A>T | GRCh38 |
| NC_000008.10:g.118909260A>T , CM000670.1:g.118909260A>T | GRCh37 |
| NC_000008.9:g.118978441A>T | NCBI36 |
| NG_007455.2:g.219799T>A , LRG_493:g.219799T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684189.1:n.430-59820T>A | ||
| ENST00000378204.7:c.963-59820T>A MANE Select | ENSP00000367446.3:n.963-59820T>A | |
| ENST00000436216.2:c.331-59820T>A | ||
| ENST00000378204.6:c.963-59820T>A | ENSP00000367446.2:n.963-59820T>A | |
| ENST00000436216.1:c.331-59820T>A | ||
| ENST00000437196.1:c.74-61470T>A | ENSP00000407299.1:n.74-61470T>A | |
| NM_000127.2:c.963-59820T>A , LRG_493t1:c.963-59820T>A | NP_000118.2:n.963-59820T>A | |
| NM_000127.3:c.963-59820T>A MANE Select | NP_000118.2:n.963-59820T>A |