Canonical Allele Identifier: CA2256579761
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs1912139613

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33448867G>C , CM000679.2:g.33448867G>C GRCh38
NC_000017.10:g.31775885G>C , CM000679.1:g.31775885G>C GRCh37
NC_000017.9:g.28799998G>C NCBI36
NG_029763.1:g.712941C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000359872.6:c.556-336800C>G ENSP00000352934.6:n.556-336800C>G
NM_001094.4:c.556-336800C>G NP_001085.2:n.556-336800C>G
NM_001094.5:c.556-336800C>G NP_001085.2:n.556-336800C>G