Canonical Allele Identifier: CA469860997
Gene:

Linked Data

dbSNP Id: rs1839460650
MyVariant Identifiers: chr10:g.59572504T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812744T>C , CM000672.2:g.57812744T>C GRCh38
NC_000010.10:g.59572504T>C , CM000672.1:g.59572504T>C GRCh37
NC_000010.9:g.59242510T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945979.1:n.68+34548A>G
XR_001747454.1:n.85+34548A>G