Canonical Allele Identifier: CA393086955
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73615523T>C (hg19) chr15:g.73323182T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323182T>C , CM000677.2:g.73323182T>C GRCh38
NC_000015.9:g.73615523T>C , CM000677.1:g.73615523T>C GRCh37
NC_000015.8:g.71402576T>C NCBI36
NG_009063.1:g.51083A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2911A>G MANE Select ENSP00000261917.3:p.Ser971Gly
ENST00000261917.3:c.2911A>G ENSP00000261917.3:p.Ser971Gly
NM_005477.2:c.2911A>G NP_005468.1:p.Ser971Gly
XM_011521148.1:c.1693A>G XP_011519450.1:p.Ser565Gly
XM_011521148.2:c.1693A>G XP_011519450.1:p.Ser565Gly
NM_005477.3:c.2911A>G MANE Select NP_005468.1:p.Ser971Gly
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