Canonical Allele Identifier: CA1595022624
Gene:

Linked Data

dbSNP Id: rs545131750

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159333053T>C , CM000667.2:g.159333053T>C GRCh38
NC_000005.9:g.158760061T>C , CM000667.1:g.158760061T>C GRCh37
NC_000005.8:g.158692639T>C NCBI36
NG_009618.1:g.2421A>G , LRG_71:g.2421A>G

Transcript Alleles

HGVS Amino-acid Change
NR_037889.1:n.745+50T>C