Canonical Allele Identifier: CA2657649598
Gene:

Linked Data

gnomAD v4: 2-1554162-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.1554162A>G , CM000664.2:g.1554162A>G GRCh38
NC_000002.11:g.1557934A>G , CM000664.1:g.1557934A>G GRCh37
NC_000002.10:g.1536941A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011510447.1:c.-1011A>G XP_011508749.1:n.-1011A>G
XM_011510448.1:c.-1011A>G XP_011508750.1:n.-1011A>G
XR_922720.1:n.85+2336T>C
XM_017005455.1:c.-1011A>G XP_016860944.1:n.-1011A>G
NR_168373.1:n.746-8A>G