Canonical Allele Identifier: CA7649006
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs771515707
ExAC: 15:73615906 G / T
gnomAD v2: 15-73615906-G-T
gnomAD v4: 15-73323565-G-T
MyVariant Identifiers: chr15:g.73615906G>T (hg19) chr15:g.73323565G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323565G>T , CM000677.2:g.73323565G>T GRCh38
NC_000015.9:g.73615906G>T , CM000677.1:g.73615906G>T GRCh37
NC_000015.8:g.71402959G>T NCBI36
NG_009063.1:g.50700C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2528C>A MANE Select ENSP00000261917.3:p.Ala843Asp
ENST00000261917.3:c.2528C>A ENSP00000261917.3:p.Ala843Asp
NM_005477.2:c.2528C>A NP_005468.1:p.Ala843Asp
XM_011521148.1:c.1310C>A XP_011519450.1:p.Ala437Asp
XM_011521148.2:c.1310C>A XP_011519450.1:p.Ala437Asp
NM_005477.3:c.2528C>A MANE Select NP_005468.1:p.Ala843Asp
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