Canonical Allele Identifier: CA2244625152

Linked Data

dbSNP Id: rs1970355501
gnomAD v4: 17-4932470-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4932470G>A , CM000679.2:g.4932470G>A GRCh38
NC_000017.10:g.4835765G>A , CM000679.1:g.4835765G>A GRCh37
NC_000017.9:g.4776545G>A NCBI36
NG_008767.2:g.5176G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000329125.6:c.-7+105G>A (GP1BA) MANE Select ENSP00000329380.5:n.-7+105G>A
ENST00000649830.1:c.-888+1872C>T (CHRNE) ENSP00000496907.1:n.-888+1872C>T
ENST00000329125.5:c.-7+105G>A (GP1BA) ENSP00000329380.5:n.-7+105G>A
ENST00000611961.1:c.-7+105G>A (GP1BA) ENSP00000484439.1:n.-7+105G>A
NM_000173.6:c.-7+105G>A (GP1BA) NP_000164.5:n.-7+105G>A
NM_000173.7:c.-7+105G>A (GP1BA) MANE Select NP_000164.5:n.-7+105G>A