Canonical Allele Identifier: CA703261294
Gene: AMN HGNC NCBI

Linked Data

dbSNP Id: rs1441889427

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922610G>C , CM000676.2:g.102922610G>C GRCh38
NC_000014.8:g.103388947G>C , CM000676.1:g.103388947G>C GRCh37
NC_000014.7:g.102458700G>C NCBI36
NG_008276.2:g.4955G>C , LRG_642:g.4955G>C

Transcript Alleles

HGVS Amino-acid Change
XM_011537202.1:c.-260G>C XP_011535504.1:n.-260G>C
XM_011537202.3:c.-260G>C XP_011535504.1:n.-260G>C
XM_024449714.1:c.18G>C XP_024305482.1:p.Trp6Cys