Canonical Allele Identifier: CA2626675962
Gene: AMN HGNC NCBI

Linked Data

gnomAD v4: 14-102928333-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102928333C>A , CM000676.2:g.102928333C>A GRCh38
NC_000014.8:g.103394670C>A , CM000676.1:g.103394670C>A GRCh37
NC_000014.7:g.102464423C>A NCBI36
NG_008276.2:g.10678C>A , LRG_642:g.10678C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000299155.10:c.208-93C>A MANE Select ENSP00000299155.6:n.208-93C>A
ENST00000299155.9:c.208-93C>A ENSP00000299155.5:n.208-93C>A
ENST00000541086.5:n.954-93C>A
NM_030943.3:c.208-93C>A , LRG_642t1:c.208-93C>A NP_112205.2:n.208-93C>A
XM_011537202.1:c.46-93C>A XP_011535504.1:n.46-93C>A
XM_011537203.1:c.46-93C>A XP_011535505.1:n.46-93C>A
XM_011537202.3:c.46-93C>A XP_011535504.1:n.46-93C>A
XM_011537203.3:c.46-93C>A XP_011535505.1:n.46-93C>A
XM_024449714.1:c.304-93C>A XP_024305482.1:n.304-93C>A
NM_030943.4:c.208-93C>A MANE Select NP_112205.2:n.208-93C>A
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