Canonical Allele Identifier: CA471740126
Gene: BAG3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.121432039G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672527G>C , CM000672.2:g.119672527G>C GRCh38
NC_000010.10:g.121432039G>C , CM000672.1:g.121432039G>C GRCh37
NC_000010.9:g.121422029G>C NCBI36
NG_016125.1:g.26158G>C , LRG_742:g.26158G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.780G>C MANE Select ENSP00000358081.4:p.Leu260=
ENST00000369085.7:c.780G>C ENSP00000358081.3:p.Leu260=
ENST00000450186.1:c.606G>C ENSP00000410036.1:p.Leu202=
NM_004281.3:c.780G>C , LRG_742t1:c.780G>C NP_004272.2:p.Leu260=
XM_005270287.1:c.780G>C XP_005270344.1:p.Leu260=
XM_005270287.2:c.780G>C XP_005270344.1:p.Leu260=
NM_004281.4:c.780G>C MANE Select NP_004272.2:p.Leu260=
Search 100 bp 5'
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