Canonical Allele Identifier: CA289878364
Gene: ASIC2 HGNC NCBI

Linked Data

dbSNP Id: rs373093791
MyVariant Identifiers: chr17:g.32306703G>C (hg19) chr17:g.33979684G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.33979684G>C , CM000679.2:g.33979684G>C GRCh38
NC_000017.10:g.32306703G>C , CM000679.1:g.32306703G>C GRCh37
NC_000017.9:g.29330816G>C NCBI36
NG_029763.1:g.182123C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000359872.6:c.555+176294C>G ENSP00000352934.6:n.555+176294C>G
NM_001094.4:c.555+176294C>G NP_001085.2:n.555+176294C>G
XR_001752840.1:n.404+7461C>G
NM_001094.5:c.555+176294C>G NP_001085.2:n.555+176294C>G
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