Canonical Allele Identifier: CA701271492
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.80070483G>C , CM000675.2:g.80070483G>C GRCh38
NC_000013.10:g.80644618G>C , CM000675.1:g.80644618G>C GRCh37
NC_000013.9:g.79542619G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011535340.1:c.335-669C>G XP_011533642.1:n.335-669C>G
XM_011535341.1:c.335-46C>G XP_011533643.1:n.335-46C>G
XR_942113.1:n.1077-46C>G