Canonical Allele Identifier: CA11949950
Gene:

Linked Data

dbSNP Id: rs2546890
gnomAD v2: 5-158759900-A-G
gnomAD v3: 5-159332892-A-G
gnomAD v4: 5-159332892-A-G
MyVariant Identifiers: chr5:g.158759900A>G (hg19) chr5:g.159332892A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159332892A>G , CM000667.2:g.159332892A>G GRCh38
NC_000005.9:g.158759900A>G , CM000667.1:g.158759900A>G GRCh37
NC_000005.8:g.158692478A>G NCBI36
NG_009618.1:g.2582T>C , LRG_71:g.2582T>C

Transcript Alleles

HGVS Amino-acid change
NR_037889.1:n.634A>G
Search 100 bp 5'
Search 100 bp 3'