Canonical Allele Identifier: CA797999034
Gene: ENAM HGNC NCBI

Linked Data

dbSNP Id: rs1464214096
gnomAD v3: 4-70628919-A-G
gnomAD v4: 4-70628919-A-G
MyVariant Identifiers: chr4:g.71494636A>G (hg19) chr4:g.70628919A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70628919A>G , CM000666.2:g.70628919A>G GRCh38
NC_000004.11:g.71494636A>G , CM000666.1:g.71494636A>G GRCh37
NG_013024.1:g.5176A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000396073.4:c.-106A>G MANE Select ENSP00000379383.4:n.-106A>G
ENST00000396073.3:c.-106A>G ENSP00000379383.3:n.-106A>G
NM_031889.2:c.-106A>G NP_114095.2:n.-106A>G
XM_006714056.2:c.-582A>G XP_006714119.1:n.-582A>G
XM_006714056.4:c.-582A>G XP_006714119.1:n.-582A>G
NM_031889.3:c.-106A>G MANE Select NP_114095.2:n.-106A>G
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