Canonical Allele Identifier: CA2626674709
Gene: AMN HGNC NCBI

Linked Data

gnomAD v4: 14-102922611-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922611T>C , CM000676.2:g.102922611T>C GRCh38
NC_000014.8:g.103388948T>C , CM000676.1:g.103388948T>C GRCh37
NC_000014.7:g.102458701T>C NCBI36
NG_008276.2:g.4956T>C , LRG_642:g.4956T>C

Transcript Alleles

HGVS Amino-acid change
XM_011537202.1:c.-259T>C XP_011535504.1:n.-259T>C
XM_011537202.3:c.-259T>C XP_011535504.1:n.-259T>C
XM_024449714.1:c.19T>C XP_024305482.1:p.Cys7Arg
Search 100 bp 5'
Search 100 bp 3'