Canonical Allele Identifier: CA402887165
Gene: HCN2 HGNC NCBI

Linked Data

dbSNP Id: rs1983894677
gnomAD v4: 19-616010-A-G
MyVariant Identifiers: chr19:g.616010A>G (hg19) chr19:g.616010A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.616010A>G , CM000681.2:g.616010A>G GRCh38
NC_000019.9:g.616010A>G , CM000681.1:g.616010A>G GRCh37
NC_000019.8:g.567010A>G NCBI36
NG_023049.1:g.22559T>C
NG_052810.1:g.31118A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000251287.3:c.2206A>G MANE Select ENSP00000251287.1:p.Met736Val
ENST00000251287.2:c.2206A>G ENSP00000251287.1:p.Met736Val
NM_001194.3:c.2206A>G NP_001185.3:p.Met736Val
NM_001194.4:c.2206A>G MANE Select NP_001185.3:p.Met736Val
Search 100 bp 5'
Search 100 bp 3'