Canonical Allele Identifier: CA715557974
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1320388335
MyVariant Identifiers: chr15:g.73622314C>T (hg19) chr15:g.73329973C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329973C>T , CM000677.2:g.73329973C>T GRCh38
NC_000015.9:g.73622314C>T , CM000677.1:g.73622314C>T GRCh37
NC_000015.8:g.71409367C>T NCBI36
NG_009063.1:g.44292G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1372-182G>A MANE Select ENSP00000261917.3:n.1372-182G>A
ENST00000261917.3:c.1372-182G>A ENSP00000261917.3:n.1372-182G>A
NM_005477.2:c.1372-182G>A NP_005468.1:n.1372-182G>A
XM_011521148.1:c.154-182G>A XP_011519450.1:n.154-182G>A
XM_011521148.2:c.154-182G>A XP_011519450.1:n.154-182G>A
NM_005477.3:c.1372-182G>A MANE Select NP_005468.1:n.1372-182G>A
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