Canonical Allele Identifier: CA1816330808

Gene: ZHX2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.122960900C= , CM000670.2:g.122960900C=	GRCh38
NC_000008.10:g.123973140C= , CM000670.1:g.123973140C=	GRCh37
NC_000008.9:g.124042321C=	NCBI36
NG_046951.1:g.184552C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000314393.6:c.*4+6872C= MANE Select	ENSP00000314709.4:n.*4+6872C=
ENST00000314393.5:c.*4+6872C=	ENSP00000314709.4:n.*4+6872C=
NM_014943.3:c.*4+6872C=	NP_055758.1:n.*4+6872C=
XM_005250836.3:c.*4+6872C=	XP_005250893.1:n.*4+6872C=
XM_005250837.3:c.*4+6872C=	XP_005250894.1:n.*4+6872C=
XM_011516931.1:c.*4+6872C=	XP_011515233.1:n.*4+6872C=
XM_011516932.1:c.*4+6872C=	XP_011515234.1:n.*4+6872C=
NM_001362797.1:c.*4+6872C=	NP_001349726.1:n.*4+6872C=
NM_014943.4:c.*4+6872C=	NP_055758.1:n.*4+6872C=
XM_005250836.5:c.*4+6872C=	XP_005250893.1:n.*4+6872C=
XM_011516932.3:c.*4+6872C=	XP_011515234.1:n.*4+6872C=
NM_014943.5:c.*4+6872C= MANE Select	NP_055758.1:n.*4+6872C=
NM_001362797.2:c.*4+6872C=	NP_001349726.1:n.*4+6872C=