Canonical Allele Identifier: CA768889934
Gene:

Linked Data

dbSNP Id: rs922733061
MyVariant Identifiers: chr2:g.41761715T>A (hg19) chr2:g.41534575T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.41534575T>A , CM000664.2:g.41534575T>A GRCh38
NC_000002.11:g.41761715T>A , CM000664.1:g.41761715T>A GRCh37
NC_000002.10:g.41615219T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939996.1:n.181+3151A>T
XR_939997.1:n.146+3151A>T
XR_939997.2:n.9529+3151A>T
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