Canonical Allele Identifier: CA5716503
Gene: BAG3 HGNC NCBI

Linked Data

dbSNP Id: rs200242752
ExAC: 10:121436238 C / G
gnomAD v2: 10-121436238-C-G
gnomAD v4: 10-119676726-C-G
MyVariant Identifiers: chr10:g.121436238C>G (hg19) chr10:g.119676726C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119676726C>G , CM000672.2:g.119676726C>G GRCh38
NC_000010.10:g.121436238C>G , CM000672.1:g.121436238C>G GRCh37
NC_000010.9:g.121426228C>G NCBI36
NG_016125.1:g.30357C>G , LRG_742:g.30357C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.1172C>G MANE Select ENSP00000358081.4:p.Ala391Gly
ENST00000369085.7:c.1172C>G ENSP00000358081.3:p.Ala391Gly
NM_004281.3:c.1172C>G , LRG_742t1:c.1172C>G NP_004272.2:p.Ala391Gly
XM_005270287.1:c.1169C>G XP_005270344.1:p.Ala390Gly
XM_005270287.2:c.1169C>G XP_005270344.1:p.Ala390Gly
NM_004281.4:c.1172C>G MANE Select NP_004272.2:p.Ala391Gly
Search 100 bp 5'
Search 100 bp 3'