Canonical Allele Identifier: CA393088731
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73615910G>C (hg19) chr15:g.73323569G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323569G>C , CM000677.2:g.73323569G>C GRCh38
NC_000015.9:g.73615910G>C , CM000677.1:g.73615910G>C GRCh37
NC_000015.8:g.71402963G>C NCBI36
NG_009063.1:g.50696C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2524C>G MANE Select ENSP00000261917.3:p.Pro842Ala
ENST00000261917.3:c.2524C>G ENSP00000261917.3:p.Pro842Ala
NM_005477.2:c.2524C>G NP_005468.1:p.Pro842Ala
XM_011521148.1:c.1306C>G XP_011519450.1:p.Pro436Ala
XM_011521148.2:c.1306C>G XP_011519450.1:p.Pro436Ala
NM_005477.3:c.2524C>G MANE Select NP_005468.1:p.Pro842Ala
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