Canonical Allele Identifier: CA798286985

Gene: ALB

Linked Data

• dbSNP Id: rs1250867884
• MyVariant Identifiers: chr4:g.74275021G>T (hg19) ; chr4:g.73409304G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409304G>T , CM000666.2:g.73409304G>T	GRCh38
NC_000004.11:g.74275021G>T , CM000666.1:g.74275021G>T	GRCh37
NC_000004.10:g.74493885G>T	NCBI36
NG_009291.1:g.10050G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.483-51G>T MANE Select	ENSP00000295897.4:n.483-51G>T
ENST00000295897.8:c.483-51G>T	ENSP00000295897.4:n.483-51G>T
ENST00000401494.7:c.138-51G>T	ENSP00000384695.3:n.138-51G>T
ENST00000415165.6:c.138-2692G>T	ENSP00000401820.2:n.138-2692G>T
ENST00000441319.5:c.489-51G>T	ENSP00000392541.1:n.489-51G>T
ENST00000476441.6:c.80-51G>T	ENSP00000423727.1:n.80-51G>T
ENST00000503124.5:c.33-51G>T	ENSP00000421027.1:n.33-51G>T
ENST00000505649.5:n.169-51G>T
ENST00000509063.5:c.483-51G>T	ENSP00000422784.1:n.483-51G>T
ENST00000514786.1:n.452-51G>T
ENST00000621085.4:c.483-51G>T	ENSP00000483421.1:n.483-51G>T
ENST00000621628.4:c.486+228G>T	ENSP00000480485.1:n.486+228G>T
NM_000477.5:c.483-51G>T	NP_000468.1:n.483-51G>T
NM_000477.6:c.483-51G>T	NP_000468.1:n.483-51G>T
NM_000477.7:c.483-51G>T MANE Select	NP_000468.1:n.483-51G>T