Canonical Allele Identifier: CA1816330879

Gene: ZHX2

Linked Data

• dbSNP Id: rs1813427977

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.122960949T>C , CM000670.2:g.122960949T>C	GRCh38
NC_000008.10:g.123973189T>C , CM000670.1:g.123973189T>C	GRCh37
NC_000008.9:g.124042370T>C	NCBI36
NG_046951.1:g.184601T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314393.6:c.*4+6921T>C MANE Select	ENSP00000314709.4:n.*4+6921T>C
ENST00000314393.5:c.*4+6921T>C	ENSP00000314709.4:n.*4+6921T>C
NM_014943.3:c.*4+6921T>C	NP_055758.1:n.*4+6921T>C
XM_005250836.3:c.*4+6921T>C	XP_005250893.1:n.*4+6921T>C
XM_005250837.3:c.*4+6921T>C	XP_005250894.1:n.*4+6921T>C
XM_011516931.1:c.*4+6921T>C	XP_011515233.1:n.*4+6921T>C
XM_011516932.1:c.*4+6921T>C	XP_011515234.1:n.*4+6921T>C
NM_001362797.1:c.*4+6921T>C	NP_001349726.1:n.*4+6921T>C
NM_014943.4:c.*4+6921T>C	NP_055758.1:n.*4+6921T>C
XM_005250836.5:c.*4+6921T>C	XP_005250893.1:n.*4+6921T>C
XM_011516932.3:c.*4+6921T>C	XP_011515234.1:n.*4+6921T>C
NM_014943.5:c.*4+6921T>C MANE Select	NP_055758.1:n.*4+6921T>C
NM_001362797.2:c.*4+6921T>C	NP_001349726.1:n.*4+6921T>C