Canonical Allele Identifier: CA393090838
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73325124-G-C
MyVariant Identifiers: chr15:g.73617465G>C (hg19) chr15:g.73325124G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73325124G>C , CM000677.2:g.73325124G>C GRCh38
NC_000015.9:g.73617465G>C , CM000677.1:g.73617465G>C GRCh37
NC_000015.8:g.71404518G>C NCBI36
NG_009063.1:g.49141C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1809C>G MANE Select ENSP00000261917.3:p.Phe603Leu
ENST00000261917.3:c.1809C>G ENSP00000261917.3:p.Phe603Leu
NM_005477.2:c.1809C>G NP_005468.1:p.Phe603Leu
XM_011521148.1:c.591C>G XP_011519450.1:p.Phe197Leu
XM_011521148.2:c.591C>G XP_011519450.1:p.Phe197Leu
NM_005477.3:c.1809C>G MANE Select NP_005468.1:p.Phe603Leu
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