Canonical Allele Identifier: CA2611160127
Gene: BAG3 HGNC NCBI

Linked Data

gnomAD v4: 10-119672700-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672700C>G , CM000672.2:g.119672700C>G GRCh38
NC_000010.10:g.121432212C>G , CM000672.1:g.121432212C>G GRCh37
NC_000010.9:g.121422202C>G NCBI36
NG_016125.1:g.26331C>G , LRG_742:g.26331C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.909+44C>G MANE Select ENSP00000358081.4:n.909+44C>G
ENST00000369085.7:c.909+44C>G ENSP00000358081.3:n.909+44C>G
ENST00000450186.1:c.735+44C>G ENSP00000410036.1:n.735+44C>G
NM_004281.3:c.909+44C>G , LRG_742t1:c.909+44C>G NP_004272.2:n.909+44C>G
XM_005270287.1:c.909+44C>G XP_005270344.1:n.909+44C>G
XM_005270287.2:c.909+44C>G XP_005270344.1:n.909+44C>G
NM_004281.4:c.909+44C>G MANE Select NP_004272.2:n.909+44C>G
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