MyVariant.info:
GRCh38
chr15:g.55289044T>A
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.55289044T>A , CM000677.2:g.55289044T>A | GRCh38 |
| NC_000015.9:g.55581242T>A , CM000677.1:g.55581242T>A | GRCh37 |
| NC_000015.8:g.53368534T>A | NCBI36 |
| NG_009103.1:g.5760A>T , LRG_96:g.5760A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000565776.2:n.76+672A>T | ||
| ENST00000697642.1:c.-23+672A>T | ENSP00000513368.1:n.-23+672A>T | |
| ENST00000697643.1:c.-232+672A>T | ENSP00000513369.1:n.-232+672A>T | |
| ENST00000336787.6:c.-143+672A>T MANE Select | ENSP00000337761.1:n.-143+672A>T | |
| ENST00000336787.5:c.-143+672A>T | ENSP00000337761.1:n.-143+672A>T | |
| ENST00000563262.5:c.-112+24995A>T | ENSP00000457595.1:n.-112+24995A>T | |
| ENST00000565776.1:n.76+672A>T | ||
| ENST00000567639.1:n.98+672A>T | ||
| NM_183235.2:c.-143+672A>T | NP_899058.1:n.-143+672A>T | |
| XM_005254576.3:c.-23+672A>T | XP_005254633.1:n.-23+672A>T | |
| XM_011521852.1:c.-359+672A>T | XP_011520154.1:n.-359+672A>T | |
| XM_011521853.1:c.-462+672A>T | XP_011520155.1:n.-462+672A>T | |
| XM_011521854.1:c.-232+672A>T | XP_011520156.1:n.-232+672A>T | |
| XM_011521855.1:c.-246+672A>T | XP_011520157.1:n.-246+672A>T | |
| XM_005254576.5:c.-23+672A>T | XP_005254633.1:n.-23+672A>T | |
| XM_011521855.3:c.-246+672A>T | XP_011520157.1:n.-246+672A>T | |
| XM_024450009.1:c.-462+672A>T | XP_024305777.1:n.-462+672A>T | |
| NM_183235.3:c.-143+672A>T MANE Select | NP_899058.1:n.-143+672A>T |