Canonical Allele Identifier: CA2581749893
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.1554200A>C , CM000664.2:g.1554200A>C GRCh38
NC_000002.11:g.1557972A>C , CM000664.1:g.1557972A>C GRCh37
NC_000002.10:g.1536979A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011510447.1:c.-973A>C XP_011508749.1:n.-973A>C
XM_011510448.1:c.-973A>C XP_011508750.1:n.-973A>C
XR_922720.1:n.85+2298T>G
XM_017005455.1:c.-973A>C XP_016860944.1:n.-973A>C
NR_168373.1:n.776A>C