Canonical Allele Identifier: CA10938552
Gene:

Linked Data

dbSNP Id: rs12134007
gnomAD v2: 1-38624116-C-T
gnomAD v3: 1-38158444-C-T
gnomAD v4: 1-38158444-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.38158444C>T , CM000663.2:g.38158444C>T GRCh38
NC_000001.10:g.38624116C>T , CM000663.1:g.38624116C>T GRCh37
NC_000001.9:g.38396703C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_947202.1:n.45-3249C>T
XR_947203.1:n.61+16730C>T
XR_947204.1:n.45-3249C>T
XR_947205.1:n.45-3249C>T
XR_001737984.1:n.45-3249C>T
XR_001737985.1:n.61+16730C>T
XR_001737986.1:n.45-3249C>T
XR_001737987.1:n.45-3249C>T
XR_002958294.1:n.45-3249C>T
XR_947205.2:n.45-3249C>T