Canonical Allele Identifier: CA487995811
Gene: AMN HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.103389037G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922700G>C , CM000676.2:g.102922700G>C GRCh38
NC_000014.8:g.103389037G>C , CM000676.1:g.103389037G>C GRCh37
NC_000014.7:g.102458790G>C NCBI36
NG_008276.2:g.5045G>C , LRG_642:g.5045G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299155.10:c.12G>C MANE Select ENSP00000299155.6:p.Leu4=
ENST00000299155.9:c.12G>C ENSP00000299155.5:p.Leu4=
NM_030943.3:c.12G>C , LRG_642t1:c.12G>C NP_112205.2:p.Leu4=
XM_011537202.1:c.-170G>C XP_011535504.1:n.-170G>C
XM_011537202.3:c.-170G>C XP_011535504.1:n.-170G>C
XM_024449714.1:c.108G>C XP_024305482.1:p.Leu36=
NM_030943.4:c.12G>C MANE Select NP_112205.2:p.Leu4=
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