Canonical Allele Identifier: CA129835838
Gene:

Linked Data

dbSNP Id: rs945445201
gnomAD v3: 5-159333059-A-C
gnomAD v4: 5-159333059-A-C
MyVariant Identifiers: chr5:g.158760067A>C (hg19) chr5:g.159333059A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159333059A>C , CM000667.2:g.159333059A>C GRCh38
NC_000005.9:g.158760067A>C , CM000667.1:g.158760067A>C GRCh37
NC_000005.8:g.158692645A>C NCBI36
NG_009618.1:g.2415T>G , LRG_71:g.2415T>G

Transcript Alleles

HGVS Amino-acid Change
NR_037889.1:n.745+56A>C
Search 100 bp 5'
Search 100 bp 3'