Canonical Allele Identifier: CA768889973
Gene:

Linked Data

dbSNP Id: rs753449182
MyVariant Identifiers: chr2:g.41761876C>T (hg19) chr2:g.41534736C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.41534736C>T , CM000664.2:g.41534736C>T GRCh38
NC_000002.11:g.41761876C>T , CM000664.1:g.41761876C>T GRCh37
NC_000002.10:g.41615380C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939996.1:n.181+2990G>A
XR_939997.1:n.146+2990G>A
XR_939997.2:n.9529+2990G>A
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