Canonical Allele Identifier: CA393086223
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73615337C>T (hg19) chr15:g.73322996C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322996C>T , CM000677.2:g.73322996C>T GRCh38
NC_000015.9:g.73615337C>T , CM000677.1:g.73615337C>T GRCh37
NC_000015.8:g.71402390C>T NCBI36
NG_009063.1:g.51269G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3097G>A MANE Select ENSP00000261917.3:p.Gly1033Ser
ENST00000261917.3:c.3097G>A ENSP00000261917.3:p.Gly1033Ser
NM_005477.2:c.3097G>A NP_005468.1:p.Gly1033Ser
XM_011521148.1:c.1879G>A XP_011519450.1:p.Gly627Ser
XM_011521148.2:c.1879G>A XP_011519450.1:p.Gly627Ser
NM_005477.3:c.3097G>A MANE Select NP_005468.1:p.Gly1033Ser
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