Canonical Allele Identifier: CA471634750
Gene: BAG3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.121432165T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672653T>C , CM000672.2:g.119672653T>C GRCh38
NC_000010.10:g.121432165T>C , CM000672.1:g.121432165T>C GRCh37
NC_000010.9:g.121422155T>C NCBI36
NG_016125.1:g.26284T>C , LRG_742:g.26284T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.906T>C MANE Select ENSP00000358081.4:p.Pro302=
ENST00000369085.7:c.906T>C ENSP00000358081.3:p.Pro302=
ENST00000450186.1:c.732T>C ENSP00000410036.1:p.Pro244=
NM_004281.3:c.906T>C , LRG_742t1:c.906T>C NP_004272.2:p.Pro302=
XM_005270287.1:c.906T>C XP_005270344.1:p.Pro302=
XM_005270287.2:c.906T>C XP_005270344.1:p.Pro302=
NM_004281.4:c.906T>C MANE Select NP_004272.2:p.Pro302=
Search 100 bp 5'
Search 100 bp 3'