Canonical Allele Identifier: CA2160048502

Gene: AMN

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102922683G= , CM000676.2:g.102922683G=	GRCh38
NC_000014.8:g.103389020G= , CM000676.1:g.103389020G=	GRCh37
NC_000014.7:g.102458773G=	NCBI36
NG_008276.2:g.5028G= , LRG_642:g.5028G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299155.10:c.-6G= MANE Select	ENSP00000299155.6:n.-6G=
ENST00000299155.9:c.-6G=	ENSP00000299155.5:n.-6G=
NM_030943.3:c.-6G= , LRG_642t1:c.-6G=	NP_112205.2:n.-6G=
XM_011537202.1:c.-187G=	XP_011535504.1:n.-187G=
XM_011537202.3:c.-187G=	XP_011535504.1:n.-187G=
XM_024449714.1:c.91G=	XP_024305482.1:p.Gly31=
NM_030943.4:c.-6G= MANE Select	NP_112205.2:n.-6G=