Canonical Allele Identifier: CA491151464
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73621944C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329603C>G , CM000677.2:g.73329603C>G GRCh38
NC_000015.9:g.73621944C>G , CM000677.1:g.73621944C>G GRCh37
NC_000015.8:g.71408997C>G NCBI36
NG_009063.1:g.44662G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1560G>C MANE Select ENSP00000261917.3:p.Leu520=
ENST00000261917.3:c.1560G>C ENSP00000261917.3:p.Leu520=
NM_005477.2:c.1560G>C NP_005468.1:p.Leu520=
XM_011521148.1:c.342G>C XP_011519450.1:p.Leu114=
XM_011521148.2:c.342G>C XP_011519450.1:p.Leu114=
NM_005477.3:c.1560G>C MANE Select NP_005468.1:p.Leu520=