Canonical Allele Identifier: CA129835799
Gene:

Linked Data

dbSNP Id: rs981967740
gnomAD v3: 5-159333038-C-T
gnomAD v4: 5-159333038-C-T
MyVariant Identifiers: chr5:g.158760046C>T (hg19) chr5:g.159333038C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159333038C>T , CM000667.2:g.159333038C>T GRCh38
NC_000005.9:g.158760046C>T , CM000667.1:g.158760046C>T GRCh37
NC_000005.8:g.158692624C>T NCBI36
NG_009618.1:g.2436G>A , LRG_71:g.2436G>A

Transcript Alleles

HGVS Amino-acid Change
NR_037889.1:n.745+35C>T
Search 100 bp 5'
Search 100 bp 3'