Canonical Allele Identifier: CA775350575

Gene: BIRC5

Linked Data

• dbSNP Id: rs1356466268
• gnomAD v3: 17-78223443-T-C
• gnomAD v4: 17-78223443-T-C
• MyVariant Identifiers: chr17:g.76219524T>C (hg19) ; chr17:g.78223443T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223443T>C , CM000679.2:g.78223443T>C	GRCh38
NC_000017.10:g.76219524T>C , CM000679.1:g.76219524T>C	GRCh37
NC_000017.9:g.73731119T>C	NCBI36
NG_029069.1:g.14248T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.340-22T>C MANE Select	ENSP00000324180.4:n.340-22T>C
ENST00000301633.8:c.409-22T>C	ENSP00000301633.3:n.409-22T>C
ENST00000350051.7:c.340-22T>C	ENSP00000324180.4:n.340-22T>C
ENST00000374948.6:c.222-22T>C	ENSP00000364086.1:n.222-22T>C
ENST00000589892.1:n.356-22T>C
ENST00000590925.6:c.*142-22T>C	ENSP00000467336.1:n.*142-22T>C
NM_001012270.1:c.222-22T>C	NP_001012270.1:n.222-22T>C
NM_001012271.1:c.409-22T>C	NP_001012271.1:n.409-22T>C
NM_001168.2:c.340-22T>C	NP_001159.2:n.340-22T>C
XR_243654.3:n.542-22T>C
XR_934452.1:n.611-22T>C
XR_243654.5:n.542-22T>C
XR_934452.3:n.611-22T>C
NM_001168.3:c.340-22T>C MANE Select	NP_001159.2:n.340-22T>C
NM_001012270.2:c.222-22T>C	NP_001012270.1:n.222-22T>C
NM_001012271.2:c.409-22T>C	NP_001012271.1:n.409-22T>C