Canonical Allele Identifier: CA31701832
Gene:

Linked Data

dbSNP Id: rs1039234382
gnomAD v2: 1-168618710-C-T
gnomAD v3: 1-168649472-C-T
gnomAD v4: 1-168649472-C-T
MyVariant Identifiers: chr1:g.168618710C>T (hg19) chr1:g.168649472C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649472C>T , CM000663.2:g.168649472C>T GRCh38
NC_000001.10:g.168618710C>T , CM000663.1:g.168618710C>T GRCh37
NC_000001.9:g.166885334C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922259.1:n.201-8197G>A
XR_922259.2:n.332-8197G>A
Search 100 bp 5'
Search 100 bp 3'