Canonical Allele Identifier: CA301962
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 190781
ClinVar RCV Id: RCV000170940
dbSNP Id: rs786205805
MyVariant Identifiers: chr15:g.73624497C>G (hg19) chr15:g.73332156C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73332156C>G , CM000677.2:g.73332156C>G GRCh38
NC_000015.9:g.73624497C>G , CM000677.1:g.73624497C>G GRCh37
NC_000015.8:g.71411550C>G NCBI36
NG_009063.1:g.42109G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1346G>C MANE Select ENSP00000261917.3:p.Cys449Ser
ENST00000261917.3:c.1346G>C ENSP00000261917.3:p.Cys449Ser
NM_005477.2:c.1346G>C NP_005468.1:p.Cys449Ser
XM_011521148.1:c.128G>C XP_011519450.1:p.Cys43Ser
XM_011521148.2:c.128G>C XP_011519450.1:p.Cys43Ser
NM_005477.3:c.1346G>C MANE Select NP_005468.1:p.Cys449Ser
Search 100 bp 5'
Search 100 bp 3'