Canonical Allele Identifier: CA393099157
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73368209-G-C
MyVariant Identifiers: chr15:g.73660550G>C (hg19) chr15:g.73368209G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73368209G>C , CM000677.2:g.73368209G>C GRCh38
NC_000015.9:g.73660550G>C , CM000677.1:g.73660550G>C GRCh37
NC_000015.8:g.71447603G>C NCBI36
NG_009063.1:g.6056C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.62C>G MANE Select ENSP00000261917.3:p.Ala21Gly
ENST00000261917.3:c.62C>G ENSP00000261917.3:p.Ala21Gly
NM_005477.2:c.62C>G NP_005468.1:p.Ala21Gly
NM_005477.3:c.62C>G MANE Select NP_005468.1:p.Ala21Gly
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Search 100 bp 3'