Canonical Allele Identifier: CA12124112
Gene:

Linked Data

dbSNP Id: rs1010254
gnomAD v2: 5-151734109-C-T
gnomAD v3: 5-152354548-C-T
gnomAD v4: 5-152354548-C-T
MyVariant Identifiers: chr5:g.151734109C>T (hg19) chr5:g.152354548C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.152354548C>T , CM000667.2:g.152354548C>T GRCh38
NC_000005.9:g.151734109C>T , CM000667.1:g.151734109C>T GRCh37
NC_000005.8:g.151714302C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944433.1:n.196+16685C>T
XR_944433.2:n.197+16685C>T
Search 100 bp 5'
Search 100 bp 3'