Canonical Allele Identifier: CA54579395
Gene:

Linked Data

dbSNP Id: rs941802190
MyVariant Identifiers: chr2:g.118837441C>T (hg19) chr2:g.118079865C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118079865C>T , CM000664.2:g.118079865C>T GRCh38
NC_000002.11:g.118837441C>T , CM000664.1:g.118837441C>T GRCh37
NC_000002.10:g.118553911C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011512305.1:c.697-2333G>A XP_011510607.1:n.697-2333G>A
XR_001739662.2:n.138+8386G>A
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