Canonical Allele Identifier: CA99710336

Gene: ALB

Linked Data

• dbSNP Id: rs77256214
• COSMIC: COSM3702635
• MyVariant Identifiers: chr4:g.74283804G>T (hg19) ; chr4:g.73418087G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418087G>T , CM000666.2:g.73418087G>T	GRCh38
NC_000004.11:g.74283804G>T , CM000666.1:g.74283804G>T	GRCh37
NC_000004.10:g.74502668G>T	NCBI36
NG_009291.1:g.18833G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1429-1G>T MANE Select	ENSP00000295897.4:n.1429-1G>T
ENST00000295897.8:c.1429-1G>T	ENSP00000295897.4:n.1429-1G>T
ENST00000401494.7:c.1084-1G>T	ENSP00000384695.3:n.1084-1G>T
ENST00000415165.6:c.853-1G>T	ENSP00000401820.2:n.853-1G>T
ENST00000476441.6:c.*708-1G>T	ENSP00000423727.1:n.*708-1G>T
ENST00000486939.1:n.82G>T
ENST00000503124.5:c.979-1G>T	ENSP00000421027.1:n.979-1G>T
ENST00000505649.5:n.976-1G>T
ENST00000509063.5:c.1429-1G>T	ENSP00000422784.1:n.1429-1G>T
ENST00000511370.1:c.962-1G>T
ENST00000621085.4:c.790-1G>T	ENSP00000483421.1:n.790-1G>T
ENST00000621628.4:c.790-1G>T	ENSP00000480485.1:n.790-1G>T
NM_000477.5:c.1429-1G>T	NP_000468.1:n.1429-1G>T
NM_000477.6:c.1429-1G>T	NP_000468.1:n.1429-1G>T
NM_000477.7:c.1429-1G>T MANE Select	NP_000468.1:n.1429-1G>T