Canonical Allele Identifier: CA1779749619

Gene: HGSNAT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43140449A= , CM000670.2:g.43140449A=	GRCh38
NC_000008.10:g.42995592A= , CM000670.1:g.42995592A=	GRCh37
NC_000008.9:g.43114749A=	NCBI36
NG_009552.1:g.5001A=

Transcript Alleles

HGVS	Amino-acid Change
NM_152419.2:c.-48A=	NP_689632.2:n.-48A=
XM_005273409.1:c.-48A=	XP_005273466.1:n.-48A=
XM_005273410.1:c.-48A=	XP_005273467.1:n.-48A=
XM_005273411.1:c.-48A=	XP_005273468.1:n.-48A=
XM_005273412.2:c.-48A=	XP_005273469.1:n.-48A=
XM_005273412.4:c.-48A=	XP_005273469.1:n.-48A=