Canonical Allele Identifier: CA1303190
Gene:

Linked Data

dbSNP Id: rs771127373
ExAC: 1:193090905 C / T
gnomAD v2: 1-193090905-C-T
gnomAD v4: 1-193121775-C-T
MyVariant Identifiers: chr1:g.193090905C>T (hg19) chr1:g.193121775C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193121775C>T , CM000663.2:g.193121775C>T GRCh38
NC_000001.10:g.193090905C>T , CM000663.1:g.193090905C>T GRCh37
NC_000001.9:g.191357528C>T NCBI36
NG_012691.1:g.4818C>T , LRG_507:g.4818C>T

Transcript Alleles

HGVS Amino-acid Change
XR_001738350.1:n.1882G>A
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