Canonical Allele Identifier: CA397314531

Linked Data

gnomAD v4: 17-4932734-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4932734G>C , CM000679.2:g.4932734G>C GRCh38
NC_000017.10:g.4836029G>C , CM000679.1:g.4836029G>C GRCh37
NC_000017.9:g.4776809G>C NCBI36
NG_008767.2:g.5440G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000329125.6:c.130G>C (GP1BA) MANE Select ENSP00000329380.5:p.Asp44His
ENST00000649830.1:c.-888+1608C>G (CHRNE) ENSP00000496907.1:n.-888+1608C>G
ENST00000329125.5:c.130G>C (GP1BA) ENSP00000329380.5:p.Asp44His
ENST00000611961.1:c.130G>C (GP1BA) ENSP00000484439.1:p.Asp44His
NM_000173.6:c.130G>C (GP1BA) NP_000164.5:p.Asp44His
NM_000173.7:c.130G>C (GP1BA) MANE Select NP_000164.5:p.Asp44His