Canonical Allele Identifier: CA99026451
Gene: ENAM HGNC NCBI

Linked Data

dbSNP Id: rs1041372247
MyVariant Identifiers: chr4:g.71494546C>T (hg19) chr4:g.70628829C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70628829C>T , CM000666.2:g.70628829C>T GRCh38
NC_000004.11:g.71494546C>T , CM000666.1:g.71494546C>T GRCh37
NG_013024.1:g.5086C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000396073.4:c.-196C>T MANE Select ENSP00000379383.4:n.-196C>T
ENST00000396073.3:c.-196C>T ENSP00000379383.3:n.-196C>T
NM_031889.2:c.-196C>T NP_114095.2:n.-196C>T
XM_006714056.4:c.-672C>T XP_006714119.1:n.-672C>T
NM_031889.3:c.-196C>T MANE Select NP_114095.2:n.-196C>T
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