Canonical Allele Identifier: CA378296765
Gene: BAG3 HGNC NCBI

Linked Data

gnomAD v4: 10-119676725-G-C
MyVariant Identifiers: chr10:g.121436237G>C (hg19) chr10:g.119676725G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119676725G>C , CM000672.2:g.119676725G>C GRCh38
NC_000010.10:g.121436237G>C , CM000672.1:g.121436237G>C GRCh37
NC_000010.9:g.121426227G>C NCBI36
NG_016125.1:g.30356G>C , LRG_742:g.30356G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.1171G>C MANE Select ENSP00000358081.4:p.Ala391Pro
ENST00000369085.7:c.1171G>C ENSP00000358081.3:p.Ala391Pro
NM_004281.3:c.1171G>C , LRG_742t1:c.1171G>C NP_004272.2:p.Ala391Pro
XM_005270287.1:c.1168G>C XP_005270344.1:p.Ala390Pro
XM_005270287.2:c.1168G>C XP_005270344.1:p.Ala390Pro
NM_004281.4:c.1171G>C MANE Select NP_004272.2:p.Ala391Pro
Search 100 bp 5'
Search 100 bp 3'