Canonical Allele Identifier: CA99026452
Gene: ENAM HGNC NCBI

Linked Data

dbSNP Id: rs899776067
MyVariant Identifiers: chr4:g.71494563G>A (hg19) chr4:g.70628846G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70628846G>A , CM000666.2:g.70628846G>A GRCh38
NC_000004.11:g.71494563G>A , CM000666.1:g.71494563G>A GRCh37
NG_013024.1:g.5103G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000396073.4:c.-179G>A MANE Select ENSP00000379383.4:n.-179G>A
ENST00000396073.3:c.-179G>A ENSP00000379383.3:n.-179G>A
NM_031889.2:c.-179G>A NP_114095.2:n.-179G>A
XM_006714056.4:c.-655G>A XP_006714119.1:n.-655G>A
NM_031889.3:c.-179G>A MANE Select NP_114095.2:n.-179G>A
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