Canonical Allele Identifier: CA11966306
Gene:

Linked Data

dbSNP Id: rs6890853
gnomAD v2: 5-35852311-G-A
gnomAD v3: 5-35852209-G-A
gnomAD v4: 5-35852209-G-A
MyVariant Identifiers: chr5:g.35852311G>A (hg19) chr5:g.35852209G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35852209G>A , CM000667.2:g.35852209G>A GRCh38
NC_000005.9:g.35852311G>A , CM000667.1:g.35852311G>A GRCh37
NC_000005.8:g.35888068G>A NCBI36
NG_009567.1:g.321G>A , LRG_74:g.321G>A

Transcript Alleles

HGVS Amino-acid Change
XR_001742634.1:n.1703+2111C>T
XR_001742635.1:n.1600+2111C>T
Search 100 bp 5'
Search 100 bp 3'