Canonical Allele Identifier: CA393088393
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73615742C>T (hg19) chr15:g.73323401C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323401C>T , CM000677.2:g.73323401C>T GRCh38
NC_000015.9:g.73615742C>T , CM000677.1:g.73615742C>T GRCh37
NC_000015.8:g.71402795C>T NCBI36
NG_009063.1:g.50864G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2692G>A MANE Select ENSP00000261917.3:p.Gly898Ser
ENST00000261917.3:c.2692G>A ENSP00000261917.3:p.Gly898Ser
NM_005477.2:c.2692G>A NP_005468.1:p.Gly898Ser
XM_011521148.1:c.1474G>A XP_011519450.1:p.Gly492Ser
XM_011521148.2:c.1474G>A XP_011519450.1:p.Gly492Ser
NM_005477.3:c.2692G>A MANE Select NP_005468.1:p.Gly898Ser
Search 100 bp 5'
Search 100 bp 3'