Canonical Allele Identifier: CA1912720805
Gene:

Linked Data

dbSNP Id: rs149326556
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812676C>T , CM000672.2:g.57812676C>T GRCh38
NC_000010.10:g.59572436C>T , CM000672.1:g.59572436C>T GRCh37
NC_000010.9:g.59242442C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945979.1:n.68+34616G>A
XR_001747454.1:n.85+34616G>A
Search 100 bp 5'
Search 100 bp 3'