Canonical Allele Identifier: CA7648897
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs756390842
ExAC: 15:73615399 C / G
gnomAD v2: 15-73615399-C-G
gnomAD v4: 15-73323058-C-G
MyVariant Identifiers: chr15:g.73615399C>G (hg19) chr15:g.73323058C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323058C>G , CM000677.2:g.73323058C>G GRCh38
NC_000015.9:g.73615399C>G , CM000677.1:g.73615399C>G GRCh37
NC_000015.8:g.71402452C>G NCBI36
NG_009063.1:g.51207G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3035G>C MANE Select ENSP00000261917.3:p.Gly1012Ala
ENST00000261917.3:c.3035G>C ENSP00000261917.3:p.Gly1012Ala
NM_005477.2:c.3035G>C NP_005468.1:p.Gly1012Ala
XM_011521148.1:c.1817G>C XP_011519450.1:p.Gly606Ala
XM_011521148.2:c.1817G>C XP_011519450.1:p.Gly606Ala
NM_005477.3:c.3035G>C MANE Select NP_005468.1:p.Gly1012Ala
Search 100 bp 5'
Search 100 bp 3'