Canonical Allele Identifier: CA966745664

Gene: AMN

Linked Data

• dbSNP Id: rs1891081527
• gnomAD v3: 14-102922677-A-G
• gnomAD v4: 14-102922677-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102922677A>G , CM000676.2:g.102922677A>G	GRCh38
NC_000014.8:g.103389014A>G , CM000676.1:g.103389014A>G	GRCh37
NC_000014.7:g.102458767A>G	NCBI36
NG_008276.2:g.5022A>G , LRG_642:g.5022A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299155.10:c.-12A>G MANE Select	ENSP00000299155.6:n.-12A>G
ENST00000299155.9:c.-12A>G	ENSP00000299155.5:n.-12A>G
NM_030943.3:c.-12A>G , LRG_642t1:c.-12A>G	NP_112205.2:n.-12A>G
XM_011537202.1:c.-193A>G	XP_011535504.1:n.-193A>G
XM_011537202.3:c.-193A>G	XP_011535504.1:n.-193A>G
XM_024449714.1:c.85A>G	XP_024305482.1:p.Ser29Gly
NM_030943.4:c.-12A>G MANE Select	NP_112205.2:n.-12A>G