Canonical Allele Identifier: CA5716277
Gene: BAG3 HGNC NCBI

Linked Data

dbSNP Id: rs749748006
ExAC: 10:121429449 C / T
gnomAD v2: 10-121429449-C-T
gnomAD v4: 10-119669937-C-T
MyVariant Identifiers: chr10:g.121429449C>T (hg19) chr10:g.119669937C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119669937C>T , CM000672.2:g.119669937C>T GRCh38
NC_000010.10:g.121429449C>T , CM000672.1:g.121429449C>T GRCh37
NC_000010.9:g.121419439C>T NCBI36
NG_016125.1:g.23568C>T , LRG_742:g.23568C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.267C>T MANE Select ENSP00000358081.4:p.Leu89=
ENST00000369085.7:c.267C>T ENSP00000358081.3:p.Leu89=
ENST00000450186.1:c.93C>T ENSP00000410036.1:p.Leu31=
NM_004281.3:c.267C>T , LRG_742t1:c.267C>T NP_004272.2:p.Leu89=
XM_005270287.1:c.267C>T XP_005270344.1:p.Leu89=
XM_005270287.2:c.267C>T XP_005270344.1:p.Leu89=
NM_004281.4:c.267C>T MANE Select NP_004272.2:p.Leu89=
Search 100 bp 5'
Search 100 bp 3'