Canonical Allele Identifier: CA2626675044
Gene: AMN HGNC NCBI

Linked Data

gnomAD v4: 14-102922684-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922684G>T , CM000676.2:g.102922684G>T GRCh38
NC_000014.8:g.103389021G>T , CM000676.1:g.103389021G>T GRCh37
NC_000014.7:g.102458774G>T NCBI36
NG_008276.2:g.5029G>T , LRG_642:g.5029G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299155.10:c.-5G>T MANE Select ENSP00000299155.6:n.-5G>T
ENST00000299155.9:c.-5G>T ENSP00000299155.5:n.-5G>T
NM_030943.3:c.-5G>T , LRG_642t1:c.-5G>T NP_112205.2:n.-5G>T
XM_011537202.1:c.-186G>T XP_011535504.1:n.-186G>T
XM_011537202.3:c.-186G>T XP_011535504.1:n.-186G>T
XM_024449714.1:c.92G>T XP_024305482.1:p.Gly31Val
NM_030943.4:c.-5G>T MANE Select NP_112205.2:n.-5G>T
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