Canonical Allele Identifier: CA2626675032

Gene: AMN

Linked Data

• gnomAD v4: 14-102922682-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102922682A>T , CM000676.2:g.102922682A>T	GRCh38
NC_000014.8:g.103389019A>T , CM000676.1:g.103389019A>T	GRCh37
NC_000014.7:g.102458772A>T	NCBI36
NG_008276.2:g.5027A>T , LRG_642:g.5027A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299155.10:c.-7A>T MANE Select	ENSP00000299155.6:n.-7A>T
ENST00000299155.9:c.-7A>T	ENSP00000299155.5:n.-7A>T
NM_030943.3:c.-7A>T , LRG_642t1:c.-7A>T	NP_112205.2:n.-7A>T
XM_011537202.1:c.-188A>T	XP_011535504.1:n.-188A>T
XM_011537202.3:c.-188A>T	XP_011535504.1:n.-188A>T
XM_024449714.1:c.90A>T	XP_024305482.1:p.Arg30=
NM_030943.4:c.-7A>T MANE Select	NP_112205.2:n.-7A>T