Canonical Allele Identifier: CA491479378
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1595837527
gnomAD v4: 15-73367965-C-A
MyVariant Identifiers: chr15:g.73660306C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367965C>A , CM000677.2:g.73367965C>A GRCh38
NC_000015.9:g.73660306C>A , CM000677.1:g.73660306C>A GRCh37
NC_000015.8:g.71447359C>A NCBI36
NG_009063.1:g.6300G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.306G>T MANE Select ENSP00000261917.3:p.Ser102=
ENST00000261917.3:c.306G>T ENSP00000261917.3:p.Ser102=
NM_005477.2:c.306G>T NP_005468.1:p.Ser102=
NM_005477.3:c.306G>T MANE Select NP_005468.1:p.Ser102=
Search 100 bp 5'
Search 100 bp 3'