Canonical Allele Identifier: CA397314625

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4932747A>G , CM000679.2:g.4932747A>G GRCh38
NC_000017.10:g.4836042A>G , CM000679.1:g.4836042A>G GRCh37
NC_000017.9:g.4776822A>G NCBI36
NG_008767.2:g.5453A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000329125.6:c.143A>G (GP1BA) MANE Select ENSP00000329380.5:p.Asp48Gly
ENST00000649830.1:c.-888+1595T>C (CHRNE) ENSP00000496907.1:n.-888+1595T>C
ENST00000329125.5:c.143A>G (GP1BA) ENSP00000329380.5:p.Asp48Gly
ENST00000611961.1:c.143A>G (GP1BA) ENSP00000484439.1:p.Asp48Gly
NM_000173.6:c.143A>G (GP1BA) NP_000164.5:p.Asp48Gly
NM_000173.7:c.143A>G (GP1BA) MANE Select NP_000164.5:p.Asp48Gly