Canonical Allele Identifier: CA2670906532
Gene: ENAM HGNC NCBI

Linked Data

gnomAD v4: 4-70628938-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70628938T>C , CM000666.2:g.70628938T>C GRCh38
NC_000004.11:g.71494655T>C , CM000666.1:g.71494655T>C GRCh37
NG_013024.1:g.5195T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000396073.4:c.-87T>C MANE Select ENSP00000379383.4:n.-87T>C
ENST00000396073.3:c.-87T>C ENSP00000379383.3:n.-87T>C
NM_031889.2:c.-87T>C NP_114095.2:n.-87T>C
XM_006714056.2:c.-563T>C XP_006714119.1:n.-563T>C
XM_006714056.4:c.-563T>C XP_006714119.1:n.-563T>C
NM_031889.3:c.-87T>C MANE Select NP_114095.2:n.-87T>C
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