Canonical Allele Identifier: CA1595022650
Gene:

Linked Data

dbSNP Id: rs1754314055

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159333101T>G , CM000667.2:g.159333101T>G GRCh38
NC_000005.9:g.158760109T>G , CM000667.1:g.158760109T>G GRCh37
NC_000005.8:g.158692687T>G NCBI36
NG_009618.1:g.2373A>C , LRG_71:g.2373A>C

Transcript Alleles

HGVS Amino-acid change
NR_037889.1:n.745+98T>G