Canonical Allele Identifier: CA563634415
Gene:

Linked Data

dbSNP Id: rs1464830427
gnomAD v2: 5-151734168-T-C
gnomAD v3: 5-152354607-T-C
gnomAD v4: 5-152354607-T-C
MyVariant Identifiers: chr5:g.151734168T>C (hg19) chr5:g.152354607T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.152354607T>C , CM000667.2:g.152354607T>C GRCh38
NC_000005.9:g.151734168T>C , CM000667.1:g.151734168T>C GRCh37
NC_000005.8:g.151714361T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_944433.1:n.196+16744T>C
XR_944433.2:n.197+16744T>C
Search 100 bp 5'
Search 100 bp 3'