Canonical Allele Identifier: CA1649498068
Gene:

Linked Data

dbSNP Id: rs1772155395

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98014435T>G , CM000668.2:g.98014435T>G GRCh38
NC_000006.11:g.98462311T>G , CM000668.1:g.98462311T>G GRCh37
NC_000006.10:g.98569032T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245563.2:n.371+44969T>G
XR_942809.1:n.371+44969T>G