Canonical Allele Identifier: CA5716504
Gene: BAG3 HGNC NCBI

Linked Data

dbSNP Id: rs770810573
ExAC: 10:121436241 C / T
gnomAD v4: 10-119676729-C-T
MyVariant Identifiers: chr10:g.121436241C>T (hg19) chr10:g.119676729C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119676729C>T , CM000672.2:g.119676729C>T GRCh38
NC_000010.10:g.121436241C>T , CM000672.1:g.121436241C>T GRCh37
NC_000010.9:g.121426231C>T NCBI36
NG_016125.1:g.30360C>T , LRG_742:g.30360C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.1175C>T MANE Select ENSP00000358081.4:p.Thr392Ile
ENST00000369085.7:c.1175C>T ENSP00000358081.3:p.Thr392Ile
NM_004281.3:c.1175C>T , LRG_742t1:c.1175C>T NP_004272.2:p.Thr392Ile
XM_005270287.1:c.1172C>T XP_005270344.1:p.Thr391Ile
XM_005270287.2:c.1172C>T XP_005270344.1:p.Thr391Ile
NM_004281.4:c.1175C>T MANE Select NP_004272.2:p.Thr392Ile
Search 100 bp 5'
Search 100 bp 3'