Canonical Allele Identifier: CA2710978174
Gene:

Linked Data

dbSNP Id: rs2113482276

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.11943665C>T , CM000668.2:g.11943665C>T GRCh38
NC_000006.11:g.11943898C>T , CM000668.1:g.11943898C>T GRCh37
NC_000006.10:g.12051884C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001743976.1:n.348-7870C>T