Canonical Allele Identifier: CA1149396896
Gene:

Linked Data

dbSNP Id: rs1571038142

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036400A>C , CM000663.2:g.2036400A>C GRCh38
NC_000001.10:g.1967839A>C , CM000663.1:g.1967839A>C GRCh37
NC_000001.9:g.1957699A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946823.1:n.773+35T>G
XR_001737845.2:n.811T>G
XR_946823.3:n.776+35T>G