Canonical Allele Identifier: CA2646644796
Gene: ABCA4 HGNC NCBI

Linked Data

gnomAD v4: 1-93997807-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.93997807T>C , CM000663.2:g.93997807T>C GRCh38
NC_000001.10:g.94463363T>C , CM000663.1:g.94463363T>C GRCh37
NC_000001.9:g.94235951T>C NCBI36
NG_009073.1:g.128343A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.6729+54A>G MANE Select ENSP00000359245.3:n.6729+54A>G
ENST00000370225.3:c.6729+54A>G ENSP00000359245.3:n.6729+54A>G
ENST00000536513.5:c.3105+54A>G ENSP00000439707.2:n.3105+54A>G
NM_000350.2:c.6729+54A>G NP_000341.2:n.6729+54A>G
NM_000350.3:c.6729+54A>G MANE Select NP_000341.2:n.6729+54A>G