Canonical Allele Identifier: CA502083030

Gene: BIRC5

Linked Data

• dbSNP Id: rs766041929
• gnomAD v3: 17-78223704-G-C
• gnomAD v4: 17-78223704-G-C
• MyVariant Identifiers: chr17:g.76219785G>C (hg19) ; chr17:g.78223704G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223704G>C , CM000679.2:g.78223704G>C	GRCh38
NC_000017.10:g.76219785G>C , CM000679.1:g.76219785G>C	GRCh37
NC_000017.9:g.73731380G>C	NCBI36
NG_029069.1:g.14509G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350051.8:c.*150G>C MANE Select	ENSP00000324180.4:n.*150G>C
ENST00000301633.8:c.*150G>C	ENSP00000301633.3:n.*150G>C
ENST00000350051.7:c.*150G>C	ENSP00000324180.4:n.*150G>C
ENST00000374948.6:c.*47G>C	ENSP00000364086.1:n.*47G>C
ENST00000589892.1:n.595G>C
NM_001012270.1:c.*47G>C	NP_001012270.1:n.*47G>C
NM_001012271.1:c.*150G>C	NP_001012271.1:n.*150G>C
NM_001168.2:c.*150G>C	NP_001159.2:n.*150G>C
XR_243654.3:n.781G>C
XR_934452.1:n.850G>C
XR_243654.5:n.781G>C
XR_934452.3:n.850G>C
NM_001168.3:c.*150G>C MANE Select	NP_001159.2:n.*150G>C
NM_001012270.2:c.*47G>C	NP_001012270.1:n.*47G>C
NM_001012271.2:c.*150G>C	NP_001012271.1:n.*150G>C