Canonical Allele Identifier: CA129835878
Gene:

Linked Data

dbSNP Id: rs931931676
MyVariant Identifiers: chr5:g.158760131G>C (hg19) chr5:g.159333123G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159333123G>C , CM000667.2:g.159333123G>C GRCh38
NC_000005.9:g.158760131G>C , CM000667.1:g.158760131G>C GRCh37
NC_000005.8:g.158692709G>C NCBI36
NG_009618.1:g.2351C>G , LRG_71:g.2351C>G

Transcript Alleles

HGVS Amino-acid change
NR_037889.1:n.745+120G>C
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