Canonical Allele Identifier: CA564436313
Gene:

Linked Data

dbSNP Id: rs1425812260
gnomAD v2: 5-158760103-T-C
MyVariant Identifiers: chr5:g.158760103T>C (hg19) chr5:g.159333095T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159333095T>C , CM000667.2:g.159333095T>C GRCh38
NC_000005.9:g.158760103T>C , CM000667.1:g.158760103T>C GRCh37
NC_000005.8:g.158692681T>C NCBI36
NG_009618.1:g.2379A>G , LRG_71:g.2379A>G

Transcript Alleles

HGVS Amino-acid change
NR_037889.1:n.745+92T>C
Search 100 bp 5'
Search 100 bp 3'