Canonical Allele Identifier: CA619080155
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1455054309
gnomAD v2: 15-73622430-G-A
gnomAD v3: 15-73330089-G-A
gnomAD v4: 15-73330089-G-A
MyVariant Identifiers: chr15:g.73622430G>A (hg19) chr15:g.73330089G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73330089G>A , CM000677.2:g.73330089G>A GRCh38
NC_000015.9:g.73622430G>A , CM000677.1:g.73622430G>A GRCh37
NC_000015.8:g.71409483G>A NCBI36
NG_009063.1:g.44176C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1372-298C>T MANE Select ENSP00000261917.3:n.1372-298C>T
ENST00000261917.3:c.1372-298C>T ENSP00000261917.3:n.1372-298C>T
NM_005477.2:c.1372-298C>T NP_005468.1:n.1372-298C>T
XM_011521148.1:c.154-298C>T XP_011519450.1:n.154-298C>T
XM_011521148.2:c.154-298C>T XP_011519450.1:n.154-298C>T
NM_005477.3:c.1372-298C>T MANE Select NP_005468.1:n.1372-298C>T
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