Canonical Allele Identifier: CA5716442
Gene: BAG3 HGNC NCBI

Linked Data

dbSNP Id: rs779474666

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672705G>T , CM000672.2:g.119672705G>T GRCh38
NC_000010.10:g.121432217G>T , CM000672.1:g.121432217G>T GRCh37
NC_000010.9:g.121422207G>T NCBI36
NG_016125.1:g.26336G>T , LRG_742:g.26336G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.909+49G>T MANE Select ENSP00000358081.4:n.909+49G>T
ENST00000369085.7:c.909+49G>T ENSP00000358081.3:n.909+49G>T
ENST00000450186.1:c.735+49G>T ENSP00000410036.1:n.735+49G>T
NM_004281.3:c.909+49G>T , LRG_742t1:c.909+49G>T NP_004272.2:n.909+49G>T
XM_005270287.1:c.909+49G>T XP_005270344.1:n.909+49G>T
XM_005270287.2:c.909+49G>T XP_005270344.1:n.909+49G>T
NM_004281.4:c.909+49G>T MANE Select NP_004272.2:n.909+49G>T