Canonical Allele Identifier: CA2626675063
Gene: AMN HGNC NCBI

Linked Data

gnomAD v4: 14-102922688-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922688G>C , CM000676.2:g.102922688G>C GRCh38
NC_000014.8:g.103389025G>C , CM000676.1:g.103389025G>C GRCh37
NC_000014.7:g.102458778G>C NCBI36
NG_008276.2:g.5033G>C , LRG_642:g.5033G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299155.10:c.-1G>C MANE Select ENSP00000299155.6:n.-1G>C
ENST00000299155.9:c.-1G>C ENSP00000299155.5:n.-1G>C
NM_030943.3:c.-1G>C , LRG_642t1:c.-1G>C NP_112205.2:n.-1G>C
XM_011537202.1:c.-182G>C XP_011535504.1:n.-182G>C
XM_011537202.3:c.-182G>C XP_011535504.1:n.-182G>C
XM_024449714.1:c.96G>C XP_024305482.1:p.Glu32Asp
NM_030943.4:c.-1G>C MANE Select NP_112205.2:n.-1G>C
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