Canonical Allele Identifier: CA393093767
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs2042921301

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329676A>G , CM000677.2:g.73329676A>G GRCh38
NC_000015.9:g.73622017A>G , CM000677.1:g.73622017A>G GRCh37
NC_000015.8:g.71409070A>G NCBI36
NG_009063.1:g.44589T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1487T>C MANE Select ENSP00000261917.3:p.Met496Thr
ENST00000261917.3:c.1487T>C ENSP00000261917.3:p.Met496Thr
NM_005477.2:c.1487T>C NP_005468.1:p.Met496Thr
XM_011521148.1:c.269T>C XP_011519450.1:p.Met90Thr
XM_011521148.2:c.269T>C XP_011519450.1:p.Met90Thr
NM_005477.3:c.1487T>C MANE Select NP_005468.1:p.Met496Thr