Canonical Allele Identifier: CA7649077
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs751080270
ExAC: 15:73616226 G / A
gnomAD v2: 15-73616226-G-A
gnomAD v4: 15-73323885-G-A
MyVariant Identifiers: chr15:g.73616226G>A (hg19) chr15:g.73323885G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323885G>A , CM000677.2:g.73323885G>A GRCh38
NC_000015.9:g.73616226G>A , CM000677.1:g.73616226G>A GRCh37
NC_000015.8:g.71403279G>A NCBI36
NG_009063.1:g.50380C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2208C>T MANE Select ENSP00000261917.3:p.Tyr736=
ENST00000261917.3:c.2208C>T ENSP00000261917.3:p.Tyr736=
NM_005477.2:c.2208C>T NP_005468.1:p.Tyr736=
XM_011521148.1:c.990C>T XP_011519450.1:p.Tyr330=
XM_011521148.2:c.990C>T XP_011519450.1:p.Tyr330=
NM_005477.3:c.2208C>T MANE Select NP_005468.1:p.Tyr736=
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