Canonical Allele Identifier: CA393086179
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs2042871525
gnomAD v3: 15-73322975-T-A
gnomAD v4: 15-73322975-T-A
MyVariant Identifiers: chr15:g.73615316T>A (hg19) chr15:g.73322975T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322975T>A , CM000677.2:g.73322975T>A GRCh38
NC_000015.9:g.73615316T>A , CM000677.1:g.73615316T>A GRCh37
NC_000015.8:g.71402369T>A NCBI36
NG_009063.1:g.51290A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3118A>T MANE Select ENSP00000261917.3:p.Ser1040Cys
ENST00000261917.3:c.3118A>T ENSP00000261917.3:p.Ser1040Cys
NM_005477.2:c.3118A>T NP_005468.1:p.Ser1040Cys
XM_011521148.1:c.1900A>T XP_011519450.1:p.Ser634Cys
XM_011521148.2:c.1900A>T XP_011519450.1:p.Ser634Cys
NM_005477.3:c.3118A>T MANE Select NP_005468.1:p.Ser1040Cys
Search 100 bp 5'
Search 100 bp 3'