Canonical Allele Identifier: CA715557983
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1373557185
MyVariant Identifiers: chr15:g.73622338A>G (hg19) chr15:g.73329997A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329997A>G , CM000677.2:g.73329997A>G GRCh38
NC_000015.9:g.73622338A>G , CM000677.1:g.73622338A>G GRCh37
NC_000015.8:g.71409391A>G NCBI36
NG_009063.1:g.44268T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1372-206T>C MANE Select ENSP00000261917.3:n.1372-206T>C
ENST00000261917.3:c.1372-206T>C ENSP00000261917.3:n.1372-206T>C
NM_005477.2:c.1372-206T>C NP_005468.1:n.1372-206T>C
XM_011521148.1:c.154-206T>C XP_011519450.1:n.154-206T>C
XM_011521148.2:c.154-206T>C XP_011519450.1:n.154-206T>C
NM_005477.3:c.1372-206T>C MANE Select NP_005468.1:n.1372-206T>C
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