Canonical Allele Identifier: CA1629207422
Gene: GCM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.53258320T>G , CM000668.2:g.53258320T>G GRCh38
NC_000006.11:g.53123118T>G , CM000668.1:g.53123118T>G GRCh37
NC_000006.10:g.53231077T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926880.1:n.1065+3382A>C
XR_926881.1:n.1069+3382A>C
XR_926882.1:n.1068+3382A>C
XR_926883.1:n.1067+3382A>C
XR_926884.1:n.1063+3382A>C
XR_926885.1:n.1070+3382A>C
XM_017011390.2:c.-304+3382A>C XP_016866879.1:n.-304+3382A>C