Canonical Allele Identifier: CA2346213827
Gene:

Linked Data

dbSNP Id: rs1568556112
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2674220C>T , CM000682.2:g.2674220C>T GRCh38
NC_000020.10:g.2654866C>T , CM000682.1:g.2654866C>T GRCh37
NC_000020.9:g.2602866C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_937210.1:n.675-3780G>A
XR_937211.1:n.674-3637G>A
XR_937210.2:n.668-3780G>A
XR_937211.2:n.666-3637G>A
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