Canonical Allele Identifier: CA15154161

Gene: ZNF638

Linked Data

• dbSNP Id: rs12612930
• gnomAD v2: 2-71525785-T-C
• gnomAD v3: 2-71298655-T-C
• gnomAD v4: 2-71298655-T-C
• MyVariant Identifiers: chr2:g.71525785T>C (hg19) ; chr2:g.71298655T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71298655T>C , CM000664.2:g.71298655T>C	GRCh38
NC_000002.11:g.71525785T>C , CM000664.1:g.71525785T>C	GRCh37
NC_000002.10:g.71379293T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000410075.5:c.-203+21901T>C	ENSP00000485608.1:n.-203+21901T>C
ENST00000466330.5:c.-85+21901T>C	ENSP00000485494.1:n.-85+21901T>C
ENST00000466975.5:c.116+21901T>C	ENSP00000485154.1:n.116+21901T>C
ENST00000494621.5:c.-217+21901T>C	ENSP00000485618.1:n.-217+21901T>C
XM_011532768.3:c.116+21901T>C	XP_011531070.2:n.116+21901T>C
XM_017003809.2:c.116+21901T>C	XP_016859298.1:n.116+21901T>C
XM_017003812.2:c.116+21901T>C	XP_016859301.1:n.116+21901T>C
XR_001738706.2:n.162+21901T>C
XR_002959264.1:n.162+21901T>C
XR_002959265.1:n.162+21901T>C
XR_002959266.1:n.162+21901T>C
XR_939678.3:n.162+21901T>C