Canonical Allele Identifier: CA294307266

Gene: BIRC5

Linked Data

• dbSNP Id: rs907451552
• gnomAD v3: 17-78223889-T-G
• gnomAD v4: 17-78223889-T-G
• MyVariant Identifiers: chr17:g.76219970T>G (hg19) ; chr17:g.78223889T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223889T>G , CM000679.2:g.78223889T>G	GRCh38
NC_000017.10:g.76219970T>G , CM000679.1:g.76219970T>G	GRCh37
NC_000017.9:g.73731565T>G	NCBI36
NG_029069.1:g.14694T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*335T>G MANE Select	ENSP00000324180.4:n.*335T>G
ENST00000301633.8:c.*335T>G	ENSP00000301633.3:n.*335T>G
ENST00000350051.7:c.*335T>G	ENSP00000324180.4:n.*335T>G
ENST00000374948.6:c.*232T>G	ENSP00000364086.1:n.*232T>G
NM_001012270.1:c.*232T>G	NP_001012270.1:n.*232T>G
NM_001012271.1:c.*335T>G	NP_001012271.1:n.*335T>G
NM_001168.2:c.*335T>G	NP_001159.2:n.*335T>G
XR_243654.3:n.966T>G
XR_934452.1:n.1035T>G
XR_243654.5:n.966T>G
XR_934452.3:n.1035T>G
NM_001168.3:c.*335T>G MANE Select	NP_001159.2:n.*335T>G
NM_001012270.2:c.*232T>G	NP_001012270.1:n.*232T>G
NM_001012271.2:c.*335T>G	NP_001012271.1:n.*335T>G