Canonical Allele Identifier: CA2635577937

Gene: GP1BA CHRNE

Linked Data

• gnomAD v4: 17-4932335-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4932335T>C , CM000679.2:g.4932335T>C	GRCh38
NC_000017.10:g.4835630T>C , CM000679.1:g.4835630T>C	GRCh37
NC_000017.9:g.4776410T>C	NCBI36
NG_008767.2:g.5041T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329125.6:c.-37T>C (GP1BA) MANE Select	ENSP00000329380.5:n.-37T>C
ENST00000649830.1:c.-888+2007A>G (CHRNE)	ENSP00000496907.1:n.-888+2007A>G
ENST00000329125.5:c.-37T>C (GP1BA)	ENSP00000329380.5:n.-37T>C
ENST00000611961.1:c.-37T>C (GP1BA)	ENSP00000484439.1:n.-37T>C
NM_000173.6:c.-37T>C (GP1BA)	NP_000164.5:n.-37T>C
NM_000173.7:c.-37T>C (GP1BA) MANE Select	NP_000164.5:n.-37T>C