Canonical Allele Identifier: CA2626674811
Gene: AMN HGNC NCBI

Linked Data

gnomAD v4: 14-102922632-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922632G>C , CM000676.2:g.102922632G>C GRCh38
NC_000014.8:g.103388969G>C , CM000676.1:g.103388969G>C GRCh37
NC_000014.7:g.102458722G>C NCBI36
NG_008276.2:g.4977G>C , LRG_642:g.4977G>C

Transcript Alleles

HGVS Amino-acid Change
XM_011537202.1:c.-238G>C XP_011535504.1:n.-238G>C
XM_011537202.3:c.-238G>C XP_011535504.1:n.-238G>C
XM_024449714.1:c.40G>C XP_024305482.1:p.Val14Leu
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