Canonical Allele Identifier: CA5716384
Gene: BAG3 HGNC NCBI

Linked Data

dbSNP Id: rs759686856
ExAC: 10:121431879 C / T
gnomAD v2: 10-121431879-C-T
gnomAD v3: 10-119672367-C-T
gnomAD v4: 10-119672367-C-T
MyVariant Identifiers: chr10:g.121431879C>T (hg19) chr10:g.119672367C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672367C>T , CM000672.2:g.119672367C>T GRCh38
NC_000010.10:g.121431879C>T , CM000672.1:g.121431879C>T GRCh37
NC_000010.9:g.121421869C>T NCBI36
NG_016125.1:g.25998C>T , LRG_742:g.25998C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.620C>T MANE Select ENSP00000358081.4:p.Ser207Phe
ENST00000369085.7:c.620C>T ENSP00000358081.3:p.Ser207Phe
ENST00000450186.1:c.446C>T ENSP00000410036.1:p.Ser149Phe
NM_004281.3:c.620C>T , LRG_742t1:c.620C>T NP_004272.2:p.Ser207Phe
XM_005270287.1:c.620C>T XP_005270344.1:p.Ser207Phe
XM_005270287.2:c.620C>T XP_005270344.1:p.Ser207Phe
NM_004281.4:c.620C>T MANE Select NP_004272.2:p.Ser207Phe
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