Canonical Allele Identifier: CA14241772
Gene:

Linked Data

dbSNP Id: rs212093
gnomAD v2: 16-16237754-A-G
gnomAD v3: 16-16143897-A-G
gnomAD v4: 16-16143897-A-G
MyVariant Identifiers: chr16:g.16237754A>G (hg19) chr16:g.16143897A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16143897A>G , CM000678.2:g.16143897A>G GRCh38
NC_000016.9:g.16237754A>G , CM000678.1:g.16237754A>G GRCh37
NC_000016.8:g.16145255A>G NCBI36
NG_028268.1:g.199321A>G
NG_028268.2:g.199321A>G

Transcript Alleles

HGVS Amino-acid change
XR_933134.1:n.145A>G
Search 100 bp 5'
Search 100 bp 3'