Canonical Allele Identifier: CA2244625114

Gene: GP1BA CHRNE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4932381T= , CM000679.2:g.4932381T=	GRCh38
NC_000017.10:g.4835676T= , CM000679.1:g.4835676T=	GRCh37
NC_000017.9:g.4776456T=	NCBI36
NG_008767.2:g.5087T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329125.6:c.-7+16T= (GP1BA) MANE Select	ENSP00000329380.5:n.-7+16T=
ENST00000649830.1:c.-888+1961A= (CHRNE)	ENSP00000496907.1:n.-888+1961A=
ENST00000329125.5:c.-7+16T= (GP1BA)	ENSP00000329380.5:n.-7+16T=
ENST00000611961.1:c.-7+16T= (GP1BA)	ENSP00000484439.1:n.-7+16T=
NM_000173.6:c.-7+16T= (GP1BA)	NP_000164.5:n.-7+16T=
NM_000173.7:c.-7+16T= (GP1BA) MANE Select	NP_000164.5:n.-7+16T=