Canonical Allele Identifier: CA491478737
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73615821C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323480C>G , CM000677.2:g.73323480C>G GRCh38
NC_000015.9:g.73615821C>G , CM000677.1:g.73615821C>G GRCh37
NC_000015.8:g.71402874C>G NCBI36
NG_009063.1:g.50785G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2613G>C MANE Select ENSP00000261917.3:p.Leu871=
ENST00000261917.3:c.2613G>C ENSP00000261917.3:p.Leu871=
NM_005477.2:c.2613G>C NP_005468.1:p.Leu871=
XM_011521148.1:c.1395G>C XP_011519450.1:p.Leu465=
XM_011521148.2:c.1395G>C XP_011519450.1:p.Leu465=
NM_005477.3:c.2613G>C MANE Select NP_005468.1:p.Leu871=
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Search 100 bp 3'