Canonical Allele Identifier: CA627637301

Gene: BIRC5

Linked Data

• dbSNP Id: rs1181074026
• gnomAD v2: 17-76221440-G-T
• gnomAD v3: 17-78225359-G-T
• gnomAD v4: 17-78225359-G-T
• MyVariant Identifiers: chr17:g.76221440G>T (hg19) ; chr17:g.78225359G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78225359G>T , CM000679.2:g.78225359G>T	GRCh38
NC_000017.10:g.76221440G>T , CM000679.1:g.76221440G>T	GRCh37
NC_000017.9:g.73733035G>T	NCBI36
NG_029069.1:g.16164G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350051.8:c.*1805G>T MANE Select	ENSP00000324180.4:n.*1805G>T
ENST00000301633.8:c.*1805G>T	ENSP00000301633.3:n.*1805G>T
ENST00000350051.7:c.*1805G>T	ENSP00000324180.4:n.*1805G>T
ENST00000374948.6:c.*1702G>T	ENSP00000364086.1:n.*1702G>T
NM_001012270.1:c.*1702G>T	NP_001012270.1:n.*1702G>T
NM_001012271.1:c.*1805G>T	NP_001012271.1:n.*1805G>T
NM_001168.2:c.*1805G>T	NP_001159.2:n.*1805G>T
XR_934452.1:n.2505G>T
XR_243654.5:n.2436G>T
XR_934452.3:n.2505G>T
NM_001168.3:c.*1805G>T MANE Select	NP_001159.2:n.*1805G>T
NM_001012270.2:c.*1702G>T	NP_001012270.1:n.*1702G>T
NM_001012271.2:c.*1805G>T	NP_001012271.1:n.*1805G>T