Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.42131063G>C , CM000684.2:g.42131063G>C | GRCh38 |
| NC_000022.10:g.42527065G>C , CM000684.1:g.42527065G>C | GRCh37 |
| NC_000022.9:g.40857009G>C | NCBI36 |
| NG_008376.3:g.3929C>G | |
| NG_008376.4:g.4748C>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XM_011529966.1:c.-272C>G | XP_011528268.1:n.-272C>G |
| XM_011529967.1:c.-272C>G | XP_011528269.1:n.-272C>G |
| XM_011529968.1:c.-272C>G | XP_011528270.1:n.-272C>G |
| XM_011529969.1:c.37+234C>G | XP_011528271.1:n.37+234C>G |
| XM_011529970.1:c.-272C>G | XP_011528272.1:n.-272C>G |
| XM_011529971.1:c.37+234C>G | XP_011528273.1:n.37+234C>G |
| XM_011529972.1:c.-272C>G | XP_011528274.1:n.-272C>G |
| XR_002958749.1:n.275+375G>C | |
| XR_430455.2:n.328+375G>C |