Canonical Allele Identifier: CA621196499
Gene:

Linked Data

dbSNP Id: rs1464443262
gnomAD v2: 16-16237660-T-C
gnomAD v3: 16-16143803-T-C
gnomAD v4: 16-16143803-T-C
MyVariant Identifiers: chr16:g.16237660T>C (hg19) chr16:g.16143803T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16143803T>C , CM000678.2:g.16143803T>C GRCh38
NC_000016.9:g.16237660T>C , CM000678.1:g.16237660T>C GRCh37
NC_000016.8:g.16145161T>C NCBI36
NG_028268.1:g.199227T>C
NG_028268.2:g.199227T>C

Transcript Alleles

HGVS Amino-acid change
XR_933134.1:n.51T>C
Search 100 bp 5'
Search 100 bp 3'