Canonical Allele Identifier: CA393097398
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73659974A>G (hg19) chr15:g.73367633A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367633A>G , CM000677.2:g.73367633A>G GRCh38
NC_000015.9:g.73659974A>G , CM000677.1:g.73659974A>G GRCh37
NC_000015.8:g.71447027A>G NCBI36
NG_009063.1:g.6632T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.638T>C MANE Select ENSP00000261917.3:p.Phe213Ser
ENST00000261917.3:c.638T>C ENSP00000261917.3:p.Phe213Ser
NM_005477.2:c.638T>C NP_005468.1:p.Phe213Ser
NM_005477.3:c.638T>C MANE Select NP_005468.1:p.Phe213Ser
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