Canonical Allele Identifier: CA2626675064

Gene: AMN

Linked Data

• gnomAD v4: 14-102922688-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102922688G>T , CM000676.2:g.102922688G>T	GRCh38
NC_000014.8:g.103389025G>T , CM000676.1:g.103389025G>T	GRCh37
NC_000014.7:g.102458778G>T	NCBI36
NG_008276.2:g.5033G>T , LRG_642:g.5033G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299155.10:c.-1G>T MANE Select	ENSP00000299155.6:n.-1G>T
ENST00000299155.9:c.-1G>T	ENSP00000299155.5:n.-1G>T
NM_030943.3:c.-1G>T , LRG_642t1:c.-1G>T	NP_112205.2:n.-1G>T
XM_011537202.1:c.-182G>T	XP_011535504.1:n.-182G>T
XM_011537202.3:c.-182G>T	XP_011535504.1:n.-182G>T
XM_024449714.1:c.96G>T	XP_024305482.1:p.Glu32Asp
NM_030943.4:c.-1G>T MANE Select	NP_112205.2:n.-1G>T