Canonical Allele Identifier: CA393089162
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73616135G>A (hg19) chr15:g.73323794G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323794G>A , CM000677.2:g.73323794G>A GRCh38
NC_000015.9:g.73616135G>A , CM000677.1:g.73616135G>A GRCh37
NC_000015.8:g.71403188G>A NCBI36
NG_009063.1:g.50471C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2299C>T MANE Select ENSP00000261917.3:p.Pro767Ser
ENST00000261917.3:c.2299C>T ENSP00000261917.3:p.Pro767Ser
NM_005477.2:c.2299C>T NP_005468.1:p.Pro767Ser
XM_011521148.1:c.1081C>T XP_011519450.1:p.Pro361Ser
XM_011521148.2:c.1081C>T XP_011519450.1:p.Pro361Ser
NM_005477.3:c.2299C>T MANE Select NP_005468.1:p.Pro767Ser
Search 100 bp 5'
Search 100 bp 3'