Canonical Allele Identifier: CA487995790

Gene: AMN

Linked Data

• gnomAD v4: 14-102922694-C-A
• MyVariant Identifiers: chr14:g.103389031C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102922694C>A , CM000676.2:g.102922694C>A	GRCh38
NC_000014.8:g.103389031C>A , CM000676.1:g.103389031C>A	GRCh37
NC_000014.7:g.102458784C>A	NCBI36
NG_008276.2:g.5039C>A , LRG_642:g.5039C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299155.10:c.6C>A MANE Select	ENSP00000299155.6:p.Gly2=
ENST00000299155.9:c.6C>A	ENSP00000299155.5:p.Gly2=
NM_030943.3:c.6C>A , LRG_642t1:c.6C>A	NP_112205.2:p.Gly2=
XM_011537202.1:c.-176C>A	XP_011535504.1:n.-176C>A
XM_011537202.3:c.-176C>A	XP_011535504.1:n.-176C>A
XM_024449714.1:c.102C>A	XP_024305482.1:p.Gly34=
NM_030943.4:c.6C>A MANE Select	NP_112205.2:p.Gly2=