Canonical Allele Identifier: CA529297686
Gene:

Linked Data

dbSNP Id: rs1204673407
gnomAD v2: 1-220664978-C-CA
gnomAD v3: 1-220491636-C-CA
gnomAD v4: 1-220491636-C-CA
MyVariant Identifiers: chr1:g.220664978_220664979insA (hg19) chr1:g.220491636_220491637insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220491636_220491637insA , CM000663.2:g.220491636_220491637insA GRCh38
NC_000001.10:g.220664978_220664979insA , CM000663.1:g.220664978_220664979insA GRCh37
NC_000001.9:g.218731601_218731602insA NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922615.1:n.256-598_256-597insA
XR_001737822.1:n.557-598_557-597insA
Search 100 bp 5'
Search 100 bp 3'