Canonical Allele Identifier: CA393098107
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs767160441

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367862C>A , CM000677.2:g.73367862C>A GRCh38
NC_000015.9:g.73660203C>A , CM000677.1:g.73660203C>A GRCh37
NC_000015.8:g.71447256C>A NCBI36
NG_009063.1:g.6403G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.409G>T MANE Select ENSP00000261917.3:p.Ala137Ser
ENST00000261917.3:c.409G>T ENSP00000261917.3:p.Ala137Ser
NM_005477.2:c.409G>T NP_005468.1:p.Ala137Ser
NM_005477.3:c.409G>T MANE Select NP_005468.1:p.Ala137Ser