Canonical Allele Identifier: CA660664691
Gene: BAG3 HGNC NCBI

Linked Data

dbSNP Id: rs1187427159
MyVariant Identifiers: chr10:g.121431690A>G (hg19) chr10:g.119672178A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672178A>G , CM000672.2:g.119672178A>G GRCh38
NC_000010.10:g.121431690A>G , CM000672.1:g.121431690A>G GRCh37
NC_000010.9:g.121421680A>G NCBI36
NG_016125.1:g.25809A>G , LRG_742:g.25809A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.508-77A>G MANE Select ENSP00000358081.4:n.508-77A>G
ENST00000369085.7:c.508-77A>G ENSP00000358081.3:n.508-77A>G
ENST00000450186.1:c.334-77A>G ENSP00000410036.1:n.334-77A>G
NM_004281.3:c.508-77A>G , LRG_742t1:c.508-77A>G NP_004272.2:n.508-77A>G
XM_005270287.1:c.508-77A>G XP_005270344.1:n.508-77A>G
XM_005270287.2:c.508-77A>G XP_005270344.1:n.508-77A>G
NM_004281.4:c.508-77A>G MANE Select NP_004272.2:n.508-77A>G
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