Canonical Allele Identifier: CA393095102
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73635949T>A (hg19) chr15:g.73343608T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73343608T>A , CM000677.2:g.73343608T>A GRCh38
NC_000015.9:g.73635949T>A , CM000677.1:g.73635949T>A GRCh37
NC_000015.8:g.71423002T>A NCBI36
NG_009063.1:g.30657A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.986A>T MANE Select ENSP00000261917.3:p.Asp329Val
ENST00000261917.3:c.986A>T ENSP00000261917.3:p.Asp329Val
NM_005477.2:c.986A>T NP_005468.1:p.Asp329Val
NM_005477.3:c.986A>T MANE Select NP_005468.1:p.Asp329Val
Search 100 bp 5'
Search 100 bp 3'