Canonical Allele Identifier: CA2581197106

Gene: AMN

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102922615C>G , CM000676.2:g.102922615C>G	GRCh38
NC_000014.8:g.103388952C>G , CM000676.1:g.103388952C>G	GRCh37
NC_000014.7:g.102458705C>G	NCBI36
NG_008276.2:g.4960C>G , LRG_642:g.4960C>G

Transcript Alleles

HGVS	Amino-acid change
XM_011537202.1:c.-255C>G	XP_011535504.1:n.-255C>G
XM_011537202.3:c.-255C>G	XP_011535504.1:n.-255C>G
XM_024449714.1:c.23C>G	XP_024305482.1:p.Pro8Arg